Research Coordinator Resume Samples

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RR
R Roob
Roel
Roob
915 Rolfson Islands
San Francisco
CA
+1 (555) 381 2062
915 Rolfson Islands
San Francisco
CA
Phone
p +1 (555) 381 2062
Experience Experience
Boston, MA
Research Coordinator
Boston, MA
Wolf, Stiedemann and Becker
Boston, MA
Research Coordinator
  • Help identify problems with clinical trial start-up and management. Assist with organized improvement efforts and developing research study design improvements
  • Works with department supervisor/manager to assist and train new hires in the research department/across all specialties
  • Works directly with faculty to design and improve data collection efforts. Manages all data collection
  • Work with the Principal Investigator (PI) to develop and update study protocols, including the development of new measures
  • Assist in background research for the proposed quality improvement projects and support toolkit development for hospitals across IL
  • Supervises research personnel and ensures orientation and training, performance management, and career development
  • Assign work; ensure proper workflow of the unit; act as lead worker
Chicago, IL
Senior Research Coordinator
Chicago, IL
Collier-Brown
Chicago, IL
Senior Research Coordinator
  • Makes recommendations for program enhancements, performance improvement, and "best practices."
  • Manage qualitative workflows and pipelines from across the network
  • Supervise the work of employees in supporting roles, including assigning workload and reporting on employee performance
  • Works collaboratively with manager to monitor metrics
  • Provides leadership for data management activities
  • Oversee and manage vendors for execution of online work as well as moderate members of community sites to ensure quality research feedback
  • Provide general administrative assistance
present
Boston, MA
Senior Clinical Research Coordinator
Boston, MA
Hodkiewicz-Mueller
present
Boston, MA
Senior Clinical Research Coordinator
present
  • Develops work flow policies and procedures for assigned trials
  • Develops work flow policies and procedures, prepares manuals and documents related to operations of the function
  • Develops study budgets and assumes grant management responsibilities
  • Assist other members by educating, providing resources and consulting on difficult protocols or projects
  • Provide direct supervision to non-exempt staff (i.e. hiring/firing, performance evaluations, disciplinary actions, approve time off, etc.)
  • Provide direct supervision to non-exempt staff (i.e. hiring/firing, performance evaluations, disciplinary
  • Plans, performs, and designs statistical analysis of findings
Education Education
Bachelor’s Degree in Healthcare
Bachelor’s Degree in Healthcare
Ashford University
Bachelor’s Degree in Healthcare
Skills Skills
  • Proven ability to produce work quickly and of high quality
  • Excellent organizational skills and demonstrated ability to complete detailed work accurately
  • Excellent oral and written communication skills, excellent knowledge of grammar and sentence structure
  • Comfortable with managing multiple projects simultaneously, with ability to switch focus between projects quickly
  • Strong work ethic, excellent organization skills, and meticulous attention to detail
  • Basic knowledge of SQL
  • Careful attention to detail and an ability to anticipate future problems
  • Ability to manage and develop new projects whilst maintaining quality across existing ones
  • 5) Demonstrated attention to detail, organizational skills, and excellent written and oral communication skills
  • Strong computer knowledge and experience with MS Office (Excel, Word, PowerPoint, Access), Outlook, and Photo Shop
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15 Research Coordinator resume templates

1

Research Coordinator Resume Examples & Samples

  • Candidates must thrive in a high-energy environment, be detail oriented and aggressively diligent
  • Must be a proactive thinker who can handle multiple projects and responsibilities at once
  • Must have both strong math acumen and analytical thinking and possess good communication skills – both face-to-face and written
  • Must have strong interpersonal skills and be able to effectively work with a diversity of teams across the organization
  • Must be well organized and able to meet tight deadlines
  • Media research knowledge and/or exposure to media research tools a plus
  • Knowledge of and passion for pop culture and reality television required
2

Research Coordinator Resume Examples & Samples

  • Work in conjunction with the Director and VP of Research on the tracking, analyzing and positioning of relevant research information (e.g. TV audience, fan base and attendance data)
  • Support Director, Research with creation of regularly issued research reports
  • Provide pertinent research information and analyses to support specific MLB business initiatives
  • Assist in the design and implementation of proprietary research studies
  • Help maintain and operate the MLB research fan panel
  • Maintain a library of media, consumer, and research information
3

Research Coordinator Resume Examples & Samples

  • General administrative duties including answering telephones, calendar scheduling, arranging drive-ons, copying and faxing, filing, and planning all travel arrangements
  • Maintain budgets for the department’s projects and admin needs, including maintaining files, vendor contracts, and research reports
  • Coordinate meetings and events
  • Sort and log mail and follow-up where necessary
  • Communicate information for SVP to executives and coordinators
  • Manage speaking engagements, publicity events and functions of SVP
  • Conduct research on request and maintain a general awareness of industry trends, formats, talent and competitive environment
  • Occasionally assist the data analyst with survey programming, data processing, and building presentation decks
  • Facilitate the NBC Intern program involvement with department
  • Cover for other department assistants as needed
  • Maintain a high level of confidentiality with commitment and dedication to the executive office
  • Minimum 1 year relevant work experience
  • Proficiency in Microsoft Office including Excel, Word, PowerPoint, and Outlook
  • Previous work experience at a studio, network or agency Experience working in a fast-paced environment
  • Knowledge of TV ratings/analyses and use of Nielsen software such as GALAXY EXPLORER
  • Some knowledge of SPSS
  • Detail-oriented and with excellent organizational skills
4

Market Research Coordinator Resume Examples & Samples

  • Planning and coordinating activities relevant to customer experience programs such as the collection and analysis of actionable insights linked to research data
  • Planning, implementation, and maintaining data collection and analysis systems in support of research efforts
  • Ensures the smooth and efficient operation of research and data collection activities, to identify common loyalty drivers and customer painpoints to assist with driving process improvement initiatives based on actionable insights
  • Acts as the primary administrative point of contact for Europe for customer experience research efforts
  • Monitors the progress of specified research activities; develops and maintains records of activities, and prepares reports as required by the business
  • Prepares and distributes research output in a user-friendly format for effective results interpretation, using appropriate techniques and tools
  • Interacts with relevant parties to ensure all aspects of specified research programs are executed within the allocated timelines
  • Ensures effective communication and collaboration with key stakeholders to identify, capture and progress program enhancement requirements, working with reporting line manager to introduce required changes
  • Gathers datafiles, reports and other associated materials or documentation, filtering same to relevant parties within specified timelines
  • Is solely responsible for capturing input from external and internal stakeholders, filtering same to reporting line manager prior to addressing same
5

Research Coordinator Resume Examples & Samples

  • Organising point to point marketing/company related trips
  • Ownership of the schedule ensuring optimum efficiency
  • Monitoring target client lists versus execution
  • Coordinating with sales people and clients
  • Organising logistics
  • Coordinating & distributing presentations & marketing materials
  • �Gate Keeper� for Client & Distribution Lists for Politics, Banks and Insurance teams
  • Monitor coverage across tiered accounts and flag/chase down any omissions/gaps
  • Ensure appropriate correlation between focus/tiered accounts & distribution lists (email//hardcopy-GRP/interactive calling)
  • Organising bespoke Team/Client/Corporate related Events incl Field Trips
  • Understanding the teams strategy & required deliverables
  • Liaising with Corporates and Clients as and when required by analyst
  • Maintaining an invite & attendance log
  • Inception through to execution
  • Corporate Events & Roadshows
  • Liaising with the Corp Events & Roadshow depts. on behalf of the team
  • Ensuring that the event is appropriately branded
  • Work with teams to prioritise 1:1 meetings & target list
  • Product
  • Assist the team with all �branding� initiatives
  • Create & update bespoke marketing packs/presentations using Powerpoint
  • Assist with formatting Research product using our in house template and styles
  • Create, update and/or format tables, charts, diagrams for inclusion in Research product
  • Maintain up to date disclosures within company models and presentations
  • Other items to include but are not limited to
  • Comprehensive understanding of all Research Systems in order to be the �Go To� person for the team
  • Registering analysts for conferences & company days
  • Ensure Dealogic (Event Manager) is up to date with regard to client meetings pre event
  • Ensure Client Portal is up to date with meeting feedback post event
  • �Gate keeper� for team calendar, ensuring the appropriate meetings/details are recorded and maps / directions are provided where required, as well as company reporting dates
  • Booking point to point team travel, providing the relevant business justifications for approval
  • Complete understanding of the in-house T&E policy & procedures
  • Claiming analyst expenses and reconciling their American Express statements on a trip by trip basis
  • Answering phones for team � accurate message taking and problem solving where needed
  • Arranging ad hoc cars and couriers
  • Maintaining company contacts/client database and email/voicemail/mailing /calling lists etc(s)
  • Provide cover to the department during periods of holiday/absences and in times of heavy work flow
  • Timely and accurate filing (electronic & hardcopy) of research and company information
  • Any general administrative duties
  • Previous Equity Research experience desirable but not essential
  • Previous, client facing dept/role strongly desirable
  • Forward thinking and proactive approach to role & responsibilities
  • Proven ability to produce work quickly and of high quality
  • Ability to manage and develop new projects whilst maintaining quality across existing ones
  • Team player who�s engaged in the business and has a high level of attention to detail & accuracy
  • Confidence using Excel (charts, basic formulas)
  • Strong presentation skills using Powerpoint (creation as well as updating)
  • Strong communication (written and verbal) skills
  • Use to working in a demanding, fast-paced environment
  • Good use of initiative and self sufficiency in both busy and quiet times
  • A flexible approach to duties and ability to work longer hours when necessary (but not regularly)
  • Professional manner
  • Timeliness
6

Research Coordinator Resume Examples & Samples

  • Ensure appropriate correlation between focus/tiered accounts & distribution lists
  • Liaising with Corporates and Clients
  • Assist the team with all 'branding' initiatives
  • Assist with formatting Research product
  • Comprehensive understanding of all Research Systems in order to be the 'Go To' person for the team
  • 'Gate keeper' for team calendar,
  • Booking point to point team travel
  • Claiming analyst expenses
  • Maintaining company contacts/client database and email/voicemail/mailing /calling lists etc
  • Timely and accurate filing of research and company information
  • Team player who's engaged in the business and has a high level of attention to detail & accuracy
  • Confidence using Excel and Powerpoint
7

CO OP Product & Research Coordinator Resume Examples & Samples

  • Ensure a high level of client service by
  • Responding to client requests and inquiries in a timely, responsive manner
  • Remaining up to date with all policies, procedures and regulatory rules as they relate to client accounts
  • Ensuring accounts are accurately documented and compliant with regulatory requirements
  • Maintaining client files and information
  • Proactively contacting clients to schedule advisor appointments
  • Researching client contact information in the event that the National Branch has not been informed by client of address or phone number changes
  • Ensure effective client administration by
  • Following up with clients on missing documentation required
  • Maintain activity logs including, but not limited to call logs, meeting logs, mail logs, etc
  • Coordinate client mailings related to changes in advisor or requests for client contact
  • Resolving issues expeditiously and accurately, escalating issues to Advisor or Manager when appropriate
  • Issuing instructions for client withdrawals, deposits, and transfers according to client or Advisor instructions
  • Ensuring all client interaction is accurately documented
  • Understanding the required documentation for all client account types
  • Supporting the growth of the branch by
  • Identifying opportunities to close unprofitable accounts and facilitating the closure
  • Reviewing processes to improve administrative efficiencies
  • Identifying opportunities to gather additional assets and/or increase revenue within the existing client base (i.e. referrals, consolidation of assets, insurance, etc.)
  • Retaining key clients by effectively communicating the National Branch value proposition
  • Providing recommendations for improvement to business processes, additional value to clients, and utilization of our Team of Experts
  • Contribute to the effective functioning of the branch team by
  • Supporting data analysis and management reporting functions
  • Building effective working relationships across the team and with various business line and corporate function contacts
  • Maintaining a high level of customer service
  • Facilitating a culture of open and honest communication
  • Actively participating and contributing to touch bases and team meetings
  • Encouraging the generation of new ideas and approaches
  • Actively sharing knowledge and experience to enhance the development of all team members
  • Developing and executing a meaningful employee development plan
  • Pleasant telephone manner and an ability to keep client conversations on track
  • Working knowledge of mutual funds
  • Working knowledge of investment and retirement planning sufficient to meet the needs of clients and to compete for the business within the current market
  • Strong MS Excel skills
  • Ability to take initiative and work independently
  • Ability to meet deadlines, and targets
  • Understanding of industry and firm compliance regulations
  • Experience as an administrative associate or sales assistant an asset
  • Experience with Dataphile is an asset
8

Research Coordinator Resume Examples & Samples

  • Assists with organizing and scheduling assessments/tests/activities to meet research objectives and study protocol compliance. Communicates with study team personnel to ensure study procedures are followed and research is performed as described in protocol. Serves as contact for subjects, study personnel, Institutional Review Board (IRB) and study sponsor
  • Participates in assessing patient eligibility. Assists in coordinating study participant activities including recruitment, screening, orientation and correspondence. Schedules subject appointments, tests, and procedures coordinating with external providers as needed. Produces reports and other materials, as directed
  • Maintains accurate, complete and timely records, including source documents, consent forms, case report forms, protocol documents, and regulatory documents, as required by sponsor and institutional guidelines
  • Assists with submission of timely, accurate, and complete study continuing review, amendments, and reportable events to IRB
  • Assists with sample collection, processing and shipment for each study
9

Research Coordinator Supervisor, CRS Resume Examples & Samples

  • 10% Supervises and coordinates all aspects of sponsor-initiated and investigator initiated research studies including subject recruitment, data collection, scheduling of study-related assessments and follow-up of enrolled subjects, and budget development and administration. Plans and staffs project operations based on proposed research activities and timelines
  • 10% Supervises staff engaged in sponsor-initiated and investigator-initiated research studies. Recruits screens, and hires staff. Performs performance evaluations and provides guidance and feedback to assigned staff. Counsels, disciplines and/or terminates employees as required
  • 10% Schedules assigns, and prioritizes workloads on a daily basis. Sets appropriate goals and deadlines. Ensures timely completion of unit’s work. Assigns and monitors progress on work assignments and special projects. Trains and demonstrates techniques or procedures to research coordinators
  • 9% Oversees the planning, organizing and scheduling of assessments/tests to meet research objectives and study protocol compliance. Communicates with study team personnel to ensure study procedures are followed and performed as described in protocol. Serves as primary contact for subjects, study personnel, Institutional Review Board (IRB) and study sponsor
  • 5% Develops and manages internal budgets as required. Authorizes expenditures and monitors reconciliation and status to ensure compliance with fiscal guidelines and regulations. Prepares and/or directs the preparation of financial reports as required. Directs ongoing purchasing activities for supplies and equipment including authorization of one-time major purchases under supervision of supervisor. Researches new equipment purchases and develops recommendations for supervisor’s consideration
  • 5% Assists in recruiting subjects for studies and determines eligibility based on study criteria. Coordinates and monitors study participant activities to include recruitment, screening, orientation and correspondence. Schedules subject appointments, tests, and procedures coordinating with external providers as needed. Produces reports, correspondence and other materials, as needed
  • 5% Has responsibility for overseeing data collection for research studies following established data collection and management procedures. Oversees collection, recording, entering and preparation of data for analysis. Performs basic and moderately complex study analysis under the direction of Principal Investigator. Oversees the collections of pertinent information from study participants through interviews, administration of tests or surveys or questionnaires, medical records review, or other collection procedures
  • 5% Oversees and ensures maintenance of accurate, complete and timely records, including consent forms, source documents, case report forms, protocol documents, and regulatory documents, as required by sponsor and institutional guidelines
  • 5% Supervises the preparation and coordination of the submission of timely, accurate,
10

Research Coordinator Resume Examples & Samples

  • Creating and updating the experiment schedule while coordinating with a team of experimenters. Scheduling subjects for appointments and explaining study details and data collection procedures
  • Collecting MRI, EEG, and behavioral data with child participants, following established data collection and management procedures to prepare, collect, record, or enter data
  • Organizing and editing and maintaining datasets, while keeping accurate and detailed records
  • Collecting pertinent information from study participants through interviews, administration of tests, surveys, or questionnaires. Interview data will be recorded on paper and electronic forms as well as video
  • Have experience working in a research study environment
  • Have excellent written and verbal communication skills
  • Have excellent problem solving skills
  • Work well as a member of a research team
  • Be able to work independently and take initiative
  • Have the ability to interact well and engage with children and families from the USC community
11

Research Coordinator, CRS Resume Examples & Samples

  • Has responsibility for data collection for research studies following established data collection and management procedures. Collects, records, enters and prepares data for analysis. Performs basic study analysis under the direction of the Principal Investigator. Collects pertinent information from study participants through interviews, administration of tests, or surveys, or questionnaires, medical records review, or other collection procedures
  • Assists with development and management of project budgets. May authorize expenditures, monitor status and reconcile budget to ensure compliance with fiscal guidelines and regulations. Prepares and/or directs the preparation of financial reports as required. May direct ongoing purchasing activities including authorization of one-time purchases with approval from investigators
  • Organizes and prepares grant proposals. Collaborates with investigators to develop research proposals. Interfaces with funding and regulatory agencies to exchange information
  • Collaborates with pharmacist or materials management personnel to maintain accurate accountability of investigational products and specimens
  • Maintains automated databases and other records for reporting and compliance purposes. Generates reports and analysis of data according to project schedules or on an ad hoc basis. Provides guidance and direction to less experienced research coordinators in these efforts
  • Orders supplies and equipment. Researches and develops recommendations for new equipment purchases
12

Field Research Coordinator Resume Examples & Samples

  • Identify existing and potential sites and examiners, including but not limited to, searches in the system database, internet searches, and call lists that meet project criteria, communicate knowledgeably about current and/or forthcoming projects in order to elicit their participation in the project
  • Complete all follow-through tasks associated with bringing a site and/or an examiner on board including, but not limited to, developing letters and emails, overseeing distribution of specific project materials, and handling agreements within 24 hours of contact
  • Develop and maintain a relationship with sites and examiners, in order to communicate the populations, numbers, and validities required for each respective project
  • Maintain contact with sites and examiners on a bi-weekly basis, dependent upon project needs and maintain a record in the system
  • Fill portion of the sample assigned on time
  • Understand the sampling matrix and assign cases that fill the requirements in the sample
  • Work with sites/examiners to resolve any issues related to test protocols. Ensure sites/examiners are given correct and timely feedback on tested cases. Acquire product knowledge for all projects assigned to assist in study assignment
  • Ability to accurately enter data and all pertinent information related to each test protocol, utilizing various internal programs implemented to facilitate test tracking
  • Research and respond to inquiries from internal/external customers. Notify Manager of impact of requests
  • Create restricted-use web sites for communicating with participating sites (e.g., Word Press, Google sites, Blog Spot) and keeps these sites updated as the project progresses
  • Background in Marketing, customer service, or recruiting
  • Self-motivated, after training can work independently while seeking feedback from supervisors
  • Moderate to advanced proficiency in Excel/Word/Access/Power point
  • Comfortable with web technologies
  • Good phone etiquette
13

Senior Research Coordinator Resume Examples & Samples

  • Customer Service
  • Provide quality frontline customer service representing EY in a positive and professional manner
  • Coordinates the disposition and/or resolution of client issues
  • Supervise the work of employees in supporting roles, including assigning workload and reporting on employee performance
  • Administrative Support
  • Provide general administrative assistance
  • Support BD initiatives (researching key targets, planning email campaigns, scheduling meetings, preparing marketing materials),
  • Process client engagements in accordance to EY Policies and Procedures,
  • Provide assistance and support to the Project Manager in problem solving, project planning and management, and development and execution of stated goals and objectives
  • Assists in the coordination, supervision, and completion of special projects, as appropriate
  • Performs miscellaneous job-related duties as assigned
  • Strong interpersonal and communication skills and the ability to work effectively with a multi-disciplinary team
  • Ability to gather data, compile information, and prepare reports
  • Ability to use independent judgment and to manage and impart confidential information
  • Ability to analyze and solve problems
  • Ability to plan, develop, and coordinate multiple projects
  • Skill in examining and re-engineering operations and procedures, formulating policy, and developing and implementing new strategies and procedures
  • Skill in organizing resources and establishing priorities
  • Ability to lead and train staff and/or students
  • Knowledge of office management principles and procedures
  • Skills in the use of database management, word processing, spreadsheet, and/or presentation software
  • Organizing and coordinating skills
  • Ability to foster a cooperative work environment
  • Strong commitment to organizational goals and customer service
  • Initiative and Enthusiasm: Take self-directed action to do the job well. Anticipate potential problems and initiate corrective actions to avoid them
14

Research Coordinator Resume Examples & Samples

  • Expert level proficiency with media related software including OSi, AdConnections, Media Audit, KANTAR Media, Google Analytics or other comparable software
  • Must be able to effectively position and sell local broadcast affiliates with creative research and out of the box thinking
  • 3-5 Years of experience working inside a small to mid-size meter-diary or local people meter market
15

Research Coordinator, Research Solutions Resume Examples & Samples

  • 60% - Schedules appointments, makes travel arrangements, handles messages, expense reports and other administrative support
  • 35% - Provides support for departmental projects and back-up for research managers as needed. Track and maintain dept invoices and budgets
  • 5% - Coordinates department events
16

Research Coordinator Resume Examples & Samples

  • Provide research support for the Office of the President
  • Research topics relevant to DATG businesses, the media industry as a whole, and a wide array of current pop culture topics and issues
  • Help execute special projects and events by providing a variety of tasks as needed
  • Write briefs, memos, talking points and help prepare presentations for the office of the president
  • Draft various forms of communications on behalf of the office of the president
  • Communicate professionally in person, by phone, and through correspondence with a wide variety of DATG internal and external contacts on behalf of the Director, Office of the President
  • Provide daily administrative support including answering phone calls, scheduling meetings, managing travel arrangements, and T&E report processing
  • 1-2 years administrative experience
  • Professional, poised, and possess outstanding written and verbal communication skills
  • Dynamic and critical-thinking mindset
  • Avid consumer of TV and media
  • Skills and experience interacting with social media
  • Demonstrated ability to handle confidential and sensitive information
  • Strong computer skills in MAC and Microsoft Office products, Word, Excel, and Outlook
  • Meticulous, attentive to detail, organized, approachable and friendly
  • Willingness to work non-standard, flexible work hours and overtime as needed; ability to serve in an “on-call” capacity
  • Ability to function with flexibility in a demanding environment with competing and changing priorities
  • Demonstrates the ability to assume responsibility without direct supervision; problem-solving skills
  • Ability to handle multiple concurrent tasks with frequent interruptions
  • Positive and committed approach to working with others to support team goals
  • Bachelor’s Degree or equivalent work experience
17

Field Research Coordinator Resume Examples & Samples

  • Bachelor's degree required, preferrably in a social science such as psychology
  • Background in marketing, recruiting, test development, and/or research & development
  • Ability to work evenings and weekends as needed
18

Research Coordinator Resume Examples & Samples

  • Job Summary: The Research Coordinator II assists the PI with formulating research objectives, contributes to design of research protocols, oversees clinical research trials, conducts quality assurance reviews. Provides assistance to PI in completing IRB and TRUE 2 and On-Core submissions. Coordinates fellows and residents who are working on research with the PI. Participate in investigator meetings as requested by PI
  • Clerical Summary: The Research Coordinator II develops clinical protocols, drafts and submits protocols for institutional review board (IRB) approval, develops informed consent forms, submits grants to funding agencies and potential corporate sponsors, develops grant budgets, maintains research accounts for clinical research projects. The Research Coordinator II communicates with collaborators in other departments and at other institutions. The Research Coordinator II develops and implements operating policies, procedures, systems and algorithms to support planned operations and ensures these are well-documented and communicated to project personnel. Prepares technical reports and papers on study plans, progress and results of research activities
  • Clinical Summary: The Research Coordinator II obtains informed consent from subjects, completes demographic data collection from subject, assists the investigator in collecting data during endoscopic procedures, assists the PI in “blinding” data for collaborators inside and outside the institution, maintains data base, de-identifies data prior to transmission to outside institutions
  • Managerial Summary: The Research Coordinator II interacts, oversees and otherwise leads a team of up to ten physician investigators working with the PI on a variety of clinical trials in a variety of settings. The Research Coordinator II presides over meetings of research staff, may organize research retreats or symposia, assists physician scientists with presentation of data at local, regional, or national meetings (including assisting in designing poster presentations or PowerPoint presentations)
  • Proven minimum 2 years experience in clinical research monitoring. Sound knowledge of all aspects of the clinical research process including but not limited to study design, start-up/closeout activities, regulatory requirements, data management
  • Experience in clinical research trials and trial protocol development. Knowledge of clinical trials components including statistics, study methodology, informed consent, eligibility, and adverse events. Success and skill at researching, analyzing, and evaluating information for preparation of clinical research protocols
  • Minimum 2 years experience in supervising and managing others with ability to set and meet goals, motivate others and hold individuals accountable for deliverables. Proven project management experience including forecasting, planning, and initiating action for successful project completion
19

Market Research Coordinator Resume Examples & Samples

  • Excel at paying close attention to detail
  • A self-starter who works well independently and can navigate within a large company with complex systems
  • Ability to synthesize and analyze data and share findings
  • Expertise with Google and Microsoft Office Suite and SurveyMonkey
  • Requires 2 years of full-time experience in addition to a post-secondary degree
  • Prefer experience with SPSS or other statistical programs
  • Prefer experience with video editing programs
20

Research Coordinator Resume Examples & Samples

  • Ensures that study is conducted as written so that scientific questions are answered
  • Conducts ongoing assessment of protocol deviations and violations
  • Participates in NCI, FDA and pharmaceutical audits and is knowledgeable of their regulations, especially concerning the reporting of Serious Adverse Events. Enters SAE into iStar for reporting to the IRB. Notifies Data Managers promptly of occurrence of SAE
  • Interacts with the monitors/auditors from the sponsoring pharmaceutical companies
21

Field Research Coordinator Resume Examples & Samples

  • Identify existing and potential examiners and sites, including but not limited to, searches in the system database, internet searches, and call lists that meet project criteria, and communicate knowledgeably about current and/or forthcoming projects in order to elicit their participation in the project
  • Complete all follow-through tasks associated with bringing a site and/or an examiner on board including, but not limited to, developing letters, overseeing mailing of specific site and examiner project materials, and handling agreements within 24 hours of examiner contact
  • Develop and maintain a relationship with examiners, in order to communicate the populations, numbers, and validities required for each respective project
  • Maintain contact with examiners on a bi-weekly basis, dependent upon project needs and maintain a record in the system
  • Bachelor’s Degree in Psychology, Education, Sociology, Communication, Business, or other closely related degree. Some Master's coursework preferred
  • Marketing, customer service, psychology, or recruiting background. Prior experience in a school or clinical setting working with assessments is preferred
  • Moderate to advanced proficiency in Excel/Word/Access. 1 year or more experience working with large databases (SQL, Oracle, etc) is preferred
  • Professional demeanor to identify and recruit examiner/sites
  • Positive, can-do attitude
22

Information & Research Coordinator Resume Examples & Samples

  • Track and process daily tax news for the purposes of posting to the Internet and converting to Folio. This material includes legislation, news releases, budget materials, and administrative materials (bulletins, guides, etc.)
  • Work with content files to manipulate their format and structure for electronic (DVD and Internet) publication
  • Provide administrative support for EY’s Tax practice knowledge databases and applications, as required
  • A post-secondary degree or diploma
  • Strong proofreading and writing skills
  • Practical knowledge of any of the following is a plus: Folio Views, Adobe FrameMaker, HTML
  • The ability to meet deadlines and process material efficiently
  • Excellent attention to detail, strong organizational skills, and flexibility
  • A high degree of comfort learning and applying new technology
  • Excellent interpersonal skills; the ability to communicate effectively, work in an office environment, and deal with clients, colleagues, and government sources professionally and effectively
  • Bilingualism is a plus
23

Research Coordinator Resume Examples & Samples

  • Assists with organizing study related activities to ensure compliance with FDA, GCP, IRB, HIPAA, SOPs, sponsor and institutional regulations and requirements. Serves as contact for subjects, study personnel, the department, the school, pharmacy and other ancillary service departments, Institutional Review Board (IRB) and study sponsor
  • Participates in assessing patient eligibility. Assists in coordinating study participant activities including recruitment, screening, orientation, correspondence, and ongoing patient education about clinical trials. Schedules subject appointments, tests and procedures with internal and external providers as needed
  • Assists with data collection, input, and analysis for research studies. Maintains accurate, complete and timely records, including source documents, consent forms, case report forms, protocol documents, and regulatory documents, as required by sponsor and institutional guidelines
  • Assists with sample collection, processing and shipment for each study. Orders supplies and equipment. Researches and develops recommendations for new equipment purchases
  • Assists in organization and preparation of grant proposals. Gathers documentation such as annual reports and detailed budgets for inclusion in proposal. Assists investigators in developing research proposals. Interfaces with funding and regulatory agencies to exchange information
24

Oncology Clinical Research Coordinator Resume Examples & Samples

  • 5+ years of nursing experience
  • CT licensed RN
  • BSN and OCN certification
  • Knowledge of current nursing/medical practice in Oncology
  • Ability to coordinate & oversee adherence to clinical trial protocols
  • Detail-oriented with good organization skills
  • Critical thinking, work independently, computer proficiency are musts
  • Familiar with contracts and budgets associated with trials $
25

Research Coordinator Resume Examples & Samples

  • Bachelor’s degree minimum educational qualification
  • Experience in learning science, publishing or education, or in market research positions in other industries or education
  • Experience in dealing with customers an advantage
26

Research Coordinator Resume Examples & Samples

  • Vehicle might be required; home visits are located ~10-20 miles from the Texas Medical Center in Houston, TX or surrounding Houston area
  • Excellent ‘people person’ with ability to interact and communicate effectively with mothers of infants
  • Must enjoy working with young infants
  • Skills in handling infants required
  • Self-directed work style and high level of motivation
  • Passionate about child development and child psychology
  • Learn and adapt quickly to changes
  • Work well under pressure
  • Proficient using a computer
  • Prior experience with computer spreadsheets and database management
27

Research Coordinator Resume Examples & Samples

  • Collects and enters data into study database
  • May coordinate and schedule research subject appointments for tests and procedures
  • Maintains records for clinical study and regulatory documents
  • May correspond with patient throughout study
  • Composes and types study correspondence and other documentation
  • May recruit, advertise,and screen for research patients
  • May assist in determining patient eligibility for research protocols
  • Performs other job related duties as assigned
28

Research Coordinator Resume Examples & Samples

  • Recruit, inform and consent parents and parent-child dyads to participate in studies
  • Set-up, initialize, collect, download and clean accelerometer (activity monitor) and GPS data from data collection
  • Responsible for survey questionnaire data entry; merging of survey and accelerometry/GPS data; and maintaining the study databases
  • Manage and supervise research assistants hired for the study, including developing training materials for research staff and providing face to face training prior to study start
  • Perform related tasks as required to complete the research protocols, including creating research study forms, databases and other tools as appropriate
  • Upload confidential participant data from devices such as PDAs, GPS monitors, and activity monitors, report research findings, work with multiple types of research collection forms, independently develop and maintain Microsoft excel spreadsheets and access databases and demonstrate proficiency with outlook email communication and documentation
  • Assist with administrative duties of research study such as audit preparation, prepare study reports, management of research budgets, monetary disbursements, complete expense reports and organize participant files
  • Network and collaborate with organizations in the community for recruitment purposes
  • Ensure research projects are managed and completed according to agreed timelines, recruitment goals and quality standards
  • Experience working with children, preferred
  • Knowledge in conducting heights, weights, GPS and CSA measurements, behavioral, and physical activity questionnaires helpful
  • Willingness needed to travel within Houston area and work some evenings or weekends
  • Skill and comfort with using PC computers including Word, Excel, Access, PowerPoint, and Survey Monkey (or equivalent) software programs a must
  • Excellent communication skills, both oral and written, and interpersonal skills with investigators, staff, and participants (parents and children)
  • Great people interaction skills to work in community to recruit participants
  • Precision in preparing physical activity materials, recording data, protocol documentation, and data entry
  • Knowledge of study methods and procedures
  • Flexibility and adaptability in work schedule and carrying out job duties, including possible evening and weekend hours
  • Fast learner, great organizational skills, resourceful, and capable of multi tasking
  • Decision making skills, problem solving skills and leadership skills
  • Detail oriented and ensures tasks are completed correctly and on time
  • Bilingual in Spanish a plus
  • Must have a car or other ways of getting to families homes and community study sites around Houston, Texas, as work is performed at the Children’s Nutrition Research Center (CNRC) and various neighborhoods in Houston
  • Must be able to lift and move required assessment and physical activity equipment and materials
  • Will take part in trip validation studies around Houston and may make home visits for data collection paired with another study staff in the future
29

Research Coordinator Resume Examples & Samples

  • Attend and pass BCM certified training on HIPAA and human subject research and consent procedures
  • Responsible for recruiting, informing and consenting parents and parent-child dyads to participate in studies
  • Computer proficiency required including, but not limited to, uploading of confidential participant data from devices such as PDAs, GPS monitors, and activity monitors, reporting of research findings, working with multiple types of research collection forms, independently developing and maintaining Microsoft excel spreadsheets and access databases and demonstrate proficiency with outlook email communication and documentation
  • Assist with administrative duties of research study such as audit preparation, assisting in preparing the study reports, management of research budgets, monetary disbursements, completing expense reports and organizing participant files
  • Networking and collaborating with organizations in the community for recruitment purposes
  • Ensure that research projects are managed and completed according to agreed timelines, recruitment goals and quality standards
  • Education Required: B.S. in exercise physiology, kinesiology, public health, health psychology or related field, required
  • Education Preferred: Masters degree with two years of work experience in field of physical activity research
  • Experience Required: One year of relevant experience in a research setting with Bachelor degree or Five years of relevant experience in a research setting without a Bachelor degree
  • Experience Preferred: Experience working with children, preferred
  • Preferred: Bilingual in Spanish a plus
  • Computer literacy with prior experience with Word, Excel, Access, PowerPoint, Survey Monkey (or equivalent)
  • Supervision: Supervised by Project Investigators and Co-Investigators
  • Working Conditions: Must have a car or other ways of getting to families homes and community study sites around Houston, Texas, as work is performed at the Children’s Nutrition Research Center (CNRC) and various neighborhoods in Houston
  • Physical Requirements: Must be able to lift and move required assessment and physical activity equipment and materials
  • Physical Risk: Will take part in trip validation studies around Houston and may make home visits for data collection paired with another study staff in the future
30

Research Coordinator Resume Examples & Samples

  • Collects and documents research data
  • Maintains records for clinical study and regulatory documents May recruit, advertise, and screen for research patients
  • Enters study data into a computerized database or case report form
  • May schedule research subject appointments for tests and procedures, such as laboratory tests, x-rays, and other studies specific for the research protocol
  • Retrieves and submits test results to appropriate party
  • Education Required: Bachelor Degree in a related field; Four years of relevant work related experience in a research setting can be substituted in lieu of a degree
31

Research Coordinator Resume Examples & Samples

  • Executes research visits as designated by specific protocol guidelines. This includes identifying subjects scheduled for clinic visits or hospitalized patients potentially eligible for enrollment and preparing for study visits (scheduling research visits, preparing documentation for visits, submitting laboratory orders, contacting subjects before visits, working with physicians and nurses and other personnel involved in study visits)
  • Conducts all testing procedures required by research coordinator as delineated in the study protocols and Manuals of Operations
  • Evaluates and formats clinical research data and transmits it to central Data Coordinating Center
  • Regularly communicates with Data Coordinating Center and responds to data queries and other requests
  • Coordinates with the pathology department and interventional radiology department in procuring and appropriately processing and shipping human specimens (tissues, serum/plasma, DNA)
  • Prepares documentation and obtains data necessary to obtain initial and continued approval for applicable research protocols. Screens for and recruits research subjects
  • Conducts patient interviews to evaluate patient eligibility in studies and conducts interviews as part of routine study visits
  • May work with research pharmacy in procuring study medications for enrolled subjects
  • Prefer fluent Spanish
  • Must be able to multi-task and meet timeline goals
  • Most important qualifications are good interpersonal skills, high attention to detail, team-goal oriented, ability to stay well organized, and ability to effectively communicate orally and in writing with study subjects, research personnel and caregivers
  • Must be computer literate and have experience using Microsoft Office software
32

Research Coordinator Resume Examples & Samples

  • Required: Bachelor's Degree in a related field; four years of relevant work related experience in a research setting can be substituted in lieu of a degree
  • Required: Two years of relevant experience in a research setting with Bachelor's degree or six years of relevant experience in a research setting without a Bachelor's degree
  • Preferred: Experience in oncology studies
  • Bilingual (Spanish/English) is a plus
  • Certification as MA or NA is a plus
  • Certification in GCP is a plus
  • Must be able to communicate effectively, both verbally and in writing
  • Experience with computer spreadsheets and database management
  • Ability to understand patient studies and protocols
  • Data entry and knowledge of electronic medical record keeping
33

Research Coordinator Resume Examples & Samples

  • Coordinates with the operating room, pathology department, and or interventional radiology department(s) in procuring and appropriately processing and shipping human specimens (tissues, serum/plasma, others)
  • Prepares documentation and obtains data necessary to obtain initial and continued approval for applicable research protocols
  • Screens for research subjects or, less commonly, may recruit and advertise for them
  • Must be computer literate and have experience using Microsoft Office software. Preferable to have experience using EPIC database for patient care records
34

Senior Research Coordinator Resume Examples & Samples

  • Plans and organizes research protocols as designated by specific protocol guidelines
  • Conducts testing procedures required by study protocol
  • Participates in designing surveys used in study protocols
  • Documents results of study data and reports to principal investigators
  • Performs literature searches and prepares literature reviews
  • May recruit, advertise, and screen for research patients
  • May conduct patient interviews to evaluate patient eligibility in study. S
  • Supervises, schedules and directs the activities of less experienced research personnel
35

Senior Research Coordinator Resume Examples & Samples

  • Some of the responsibilities include accurate data collection, documentation, organization, oversight of the safety of study volunteers, and communication with volunteers’ families
  • Oversees local regulatory (IRB) requirements and maintains close communication with extramural study investigators, pharmaceutical sponsors and Therapeutic Development Center
  • Assists the investigator in the overall conduct of clinical trials as assigned
  • Ensures conduct of assigned studies is in accordance with good clinical practice, federal regulations and institutional policies
  • Communicates verbally and in writing as needed or as requested by the principal investigator of the study
  • Participates in protocol feasibility assessment and actively participates in protocol meetings including but not limited to investigator and site initiation meetings
  • Assists in training other support staff in study coordination
  • Participates in protocol monitoring, audits and follow up in coordination with other research staff
  • Maintains contact with other institutions participating in the studies
  • Prepares study related tools and assist principal investigator in reviewing treatment and visit order sets
  • Interacts with sponsors as required to facilitate protocol activities and maintain current study documents
  • Conducts research subject recruitment, screening, and enrollment
  • Conducts subject interviews to evaluate eligibility and continued participation in the study
  • Participates in subject consent process
  • Performs research related procedures as required (e.g.: blood draw, ECG, EEG, spirometry, sweat testing, questionnaires, etc.)
  • Conducts subject research study education as required within the scope of practice
  • Develops and maintains a processing and tracking system for all paperwork
  • Submit serious adverse event reporting and follow up as needed
  • Evaluates and analyzes clinical research data as appropriate
  • Interacts with patients to clarify data
36

Senior Research Coordinator Resume Examples & Samples

  • May conduct patient interviews to evaluate patient eligibility in study
  • Education Required: Bachelor's degree in a related field or four (4) years of directly related work experience in lieu of a degree
  • Experience Required: Five years of relevant experience in addition to any educational requirements
37

Development Research Coordinator Resume Examples & Samples

  • Master's degree and three years of professional experience in fundraising, communications, program management or a related function
  • Professional experience in a complex fund raising, communications, or program management role
  • Development experience in a complex institutional environment such as a university or other large organization is desirable
  • Sophisticated project management, organizational, and communications skills
  • Ability to stay on top of multiple complex projects
  • Ability to communicate confidently and professionally with a wide variety of constituents, including university administrators, donors, development and institute leadership, and colleagues
  • Flexibility to handle ad hoc assignments and accompanying deadlines
  • Demonstrated familiarity with corporate and foundation philanthropy in policy work (in an organization such as an advocacy organization, think tank, or academic public policy school/department/center)
  • Familiarity with key issues and decision-making processes in public policy, with interest or experience in environmental issues a plus
  • Good judgment in handling sensitive and confidential information and issues on a routine basis
38

Assistant Clinical Research Coordinator Resume Examples & Samples

  • Familiarity with Autism and Learning Disabilities resources in the Bay Area
  • Basic computer skills and demonstrated experience with office software and email applications
  • Ability to follow through and complete assigned tasks
39

Assistant Clinical Research Coordinator Resume Examples & Samples

  • Prior clinical or research experience, including undergraduate experience
  • Strong proficiency in Microsoft Word and Excel
  • Demonstrated ability to work independently with minimal supervision, as well as cooperatively in a team environment
  • Excellent organization, communication, and problem-solving skills
  • Ability to work effectively with a wide range of individuals and groups at all levels of authority
  • A proven capacity to set priorities, coordinate multiple assignments, work in a fast-paced, multi-tasked environment, exercising sound judgment in setting priorities with a strong attention to detail
  • Experience working with health care professionals and clinical research participants
40

Assistant Clinical Research Coordinator Resume Examples & Samples

  • Knowledge of Epidermolysis bullosa
  • Experience working with children and families dealing with complex medical conditions
  • Bachelor's degree in a related field or an equivalent combination of related education and relevant experience
41

Clinical Research Coordinator Float Replacement Resume Examples & Samples

  • Strong organizational skills and a demonstrated ability to work independently with minimal supervision as well as cooperatively in a team environment
  • Bachelor's degree in a related field or an equivalent combination of related education and relevant experience required
  • One year of relevant experience desired
42

Research Coordinator Resume Examples & Samples

  • Coordinate D & L Fellows staff acquisition activities—development of job descriptions, interview to hire process, including VU Hire-A-Dore specifications and coordination with Dr. Nwankwo, the English Department’s Administrative Assistant and WWG Research Project Coordinator
  • Supervise all Discovery & Learning Fellows working across all projects
  • Monitor activities and provide guidance to D & L Fellows Coordinators on all WWG Projects
  • Maintain regular contact with Lead Organizer, Lead Collaborators, faculty, staff, D&L Fellows and external collaborators by email, telephone, text messaging, web conferencing or Project Based software
  • Create, manage and monitor team activities on a project software application (Basecamp) or other project management application to assure benchmarks are achieved according to the project timeline
  • Provide verification of all D & L Fellows completed assignments for Approvers of the D & L Fs ETimecard submitted to VU Student Employment Services
  • Monitor financial procurement documentation and financial reports to ensure there are no budget overruns, working in conjunction with the English Department’s Administrative Assistant and Dr. Nwankwo
  • Provide oversight and maintenance of the Cloud storage files, physical files, materials, other documentation and product deliverables by curating, collecting, compiling, and organizing data in conjunction with the D & L Fellows, Dr. Nwankwo and other relevant individuals
  • Coordinate/manage meetings (In-person, teleconferences, web-based conferencing) for all project collaborators, internal and external in conjunction with Research Assistant
  • Coordinate all logistical aspects for planning public events and exhibitions in conjunction with the D & L Fellows, Dr. Nwankwo, and other relevant individuals or organizations
  • Write monthly Progress Reports and other reporting to communicate projects progression or issues
  • Coordinate accessibility to historical project files, documents, materials
  • Proposal coordination – administering proposal process in conjunction with Dr. Nwankwo and other relevant individuals
  • Other Administrative tasks: Financial report monitoring, D& L Fellows tasks/hours worked verification, supplies and materials procurement, travel coordination, community relationship building activities and other reasonable tasks assigned by the Lead Organizer
  • Submit invoices for payment of services from external individuals, vendors, contractors to Vanderbilt University Procurement Services monthly
43

Research Coordinator Resume Examples & Samples

  • Assisting in diverse ways with the analysis and presentation/communication of social science research to a broad array of audiences
  • Updating the content and interface of the research project’s website
  • Advising and assisting in the development of public relations and social media strategies for the dissemination of results and to connect with broader audiences
  • Managing subscriptions to and helping to grant access to LAPOP data
  • Sending reports by email and regular mail to project supporters, libraries, and others
  • Conducting descriptive analysis (percentages, means, cross tabulations), along with the production of graphs to describe data for placement in press releases, on websites, and in other communications
  • Working independently and with Vanderbilt’s Creative Services to generate infographics and other visual representations of data for reports, social media, and the web
  • Proofing and editing of reports and presentations, especially those directed toward policy makers, the general public, and the media
  • Writing press releases in both English and Spanish in collaboration with the Vanderbilt news and communications office
  • Creating internal reports, managing and cataloging project files
  • Assisting with the day to day administrative operations of the LAPOP research unit
  • Bachelor's degree and 5 years of experience or the equivalent required. Master’s in communications (journalism), public policy, or the social sciences preferred
  • Ability to write and communicate clearly and accurately in both English and in Spanish is required
  • The ability to understand and communicate about social science research is important
  • Knowledge of statistical analysis and software is a plus
  • Familiarity with Windows, Excel and Word is required
  • Familiarity with web design, social media techniques, and press release development is essential
  • Willingness and ability to travel domestically and abroad, only on occasion and for short periods of time (generally no more than 1-2 days) to carry out tasks related to research outreach
44

Clinical Research Coordinator, Senior Resume Examples & Samples

  • Master’s degree in a field appropriate to the area of assignment AND three years related research experience; OR, bachelor’s degree in a field appropriate to the area of assignment and four years related research experience
  • Bilingual preferred (Spanish, Navajo/Diné Bazaad, other)
  • Previous human subjects training (e.g., CITI certification) and four years’ experience as a research coordinator with direct recruitment and enrollment responsibilities
  • Current Certified Clinical Research Professional (CCRP) status
  • Self-motivated, willing and able take initiative
45

Research Coordinator Resume Examples & Samples

  • Maintain the lab budget and purchasing records
  • Responsible for the overall operation and administration of the laboratory, including technical oversight of personnel
  • Review, conduct, provide and maintain all training records of laboratory personnel
  • Write, update, and maintain SOP manuals
  • Maintain compliance with NIH Public Access Policy
  • Maintain all biological, chemical, radiation, and laser safety audits
  • Handle all security documents
  • Schedule lab equipment use for staff and collaborators
  • Purchase/inventory lab supplies
  • Express active interest in independently learning scientific background and current research performed in the lab
  • Assist in preparation and publication of scientific manuscripts
  • Become proficient with the grant submission and update requirements
  • B.S. or B.A. degree
  • Ability to learn new online protocols for the submission and updating of grants
  • Highly motivated and organized in record keeping
  • Background and hands on experience in laboratory, veterinary, or clinical settings in regards to federal, state and university regulations
  • Background in supervising technical and non-technical staff
  • Creative thinking skills
46

Research Coordinator Resume Examples & Samples

  • Scheduling research activities
  • Presenting at conferences and workshops
  • Working with the Human Subjects Protection Program to ensure compliance with all human subjects requirements
  • M.A. in Special Education, Education of Deaf/Hard of Hearing (DHH) or related field
  • Ability to work with young DHH children
  • Proficiency in American Sign Language and English
  • Knowledge of language and literacy development in young children who are DHH
  • Demonstrated ability working in a team setting and/or with a team of researchers
  • Teaching Certification
47

Research Coordinator Resume Examples & Samples

  • Strong decision making ability
  • Time management and organization skills
  • Ability to prioritize and work with leadership to operationalize tasks
  • Strong computer skills and knowledge in lab information systems
  • Advanced proficiency in Microsoft Office, specifically Excel and Access
  • Excellent oral written communication skills
  • Experience in a research laboratory preferred
  • Experience with grant submissions and grant submission software
  • Experience preparing, tracking and managing budgets and financial reports
48

Research Coordinator Resume Examples & Samples

  • Oversee and contribute to the design study questions, protocol, and materials, including structured interviews, recruitment flyers, and data collection protocols
  • Coordinate study team in conducting 60 minute structured pre-, post- and follow-up assessments with study participants
  • Help establish, formalize, and maintain relationships with community organizations, hospitals, clinics, etc. for recruitment and collaboration
  • Oversee IRB application process for all project components and work with research team to ensure all IRB requirements are met
  • Oversee the hiring, training and supervision of student study assessment team
  • Deliver mindfulness-based stress and self-compassion intervention to study participants
  • Conduct and direct regular, ongoing communication of research team; develop meeting agendas; attend meetings and take and disseminate meeting minutes; ensure investigator and staff follow-up on assigned action items
  • Other duties, as assigned
  • Certified in delivering mindfulness-based child birth or stress-management program
  • A minimum of five years’ experience in psychology, public health or social sciences research, including experience in coordinating complex research projects
  • Demonstrated qualitative and quantitative analytical skills; experience conducting literature searches and preparing literature reviews; experience in data analysis using spreadsheet software, such as MS Excel
  • Demonstrated ability to describe research projects and represent projects and colleagues in a professional and congenial manner with professional colleagues within academia and within public and private organizations outside of academia. -Demonstrated oral presentation skills, both with and without Microsoft PowerPoint. -Excellent written communication skills
  • Experience working with members of community organizations
  • Experience in planning, organizing, and facilitating research team meetings to achieve specific objectives
  • Experience in planning and organizing large meetings of people from various professional backgrounds including setting meeting goals and objectives; developing meeting sessions designed to advance objectives for specific research projects; and ensuring that appropriate investigators and researchers are brought together for specific agenda items
  • Ability to work independently with limited supervision, and to work as part of a team. Ability to balance multiple demands simultaneously under time constraints
  • Ability to exercise sound judgment and to address complex situations with creativity
  • Ability to communicate well with people from diverse ethnic/racial and socioeconomic backgrounds
  • Highly organized and attentive to detail; ability to balance multiple demands simultaneously under time constraints
  • Proficiency in MS Word, Excel, and PowerPoint
  • Flexibility might be needed in work schedule due to the nature of two-state research project (California & Washington)
49

Research Coordinator Resume Examples & Samples

  • Collaborate with faculty to write and develop study protocols. Manages the approval and implementation of research protocols, and work with process partners to ensure all protocol requirements are met
  • Monitor patient adherence to the protocol by providing compliance and study calendars. Take action to correct problems such as deviation from protocol requirements and maintain all reporting requirements
  • Recruit and screen human subjects for the study
  • Collect all case report forms, patient charts, images, radiographs, pathology specimens, and other clinical data of human subjects
  • Administer Neurocognitive Tests and Quality of Life Questionnaires to the study patients per protocol requirements
  • Communicate with external patients and referring physicians who are interested in enrolling patients to the study. Provide timely and actuate information to all internal and external inquiries
  • Submit and maintain regulatory requirements of the trial, and protocols. Meet deadlines for amendments and annual reviews; issue reports for compliance and study deviations to all review boards, including the Institutional Review Board (IRB)
  • Oversee the required documentation for participation of all UW-affiliated medical institutions, such as investigator information, site certifications, annual accrual figures, and any other procedural requirements
  • Manage clinical research budget and track billing charges; ensure correct charges go to study as required; catalog and document review of charges to protocols as needed
  • Develop reports and maintain direct communication with faculty members, UW departments, funding sponsors, and research collaborators regarding study overall research plan
  • Help identify problems with clinical trial start-up and management. Assist with organized improvement efforts and developing research study design improvements
  • Works directly with faculty to design and improve data collection efforts. Manages all data collection
  • Collaborates and assists with investigators to write manuscripts, articles, abstracts and research reports for publication in peer-reviewed journals
50

Research Coordinator Resume Examples & Samples

  • Demonstrated success managing national, longitudinal human subjects studies
  • Experience with UW research and fiscal offices and proficiency with UW systems, including SAGE, Granttracker, MyFinancial Desktop, and Ariba
  • Knowledge of social media use for business and professional communication/marketing
51

Research Coordinator Resume Examples & Samples

  • Coordinates the implementation and conduct of research projects ensuring adherence to research protocol requirements including: timely completion and communication of regulatory documents, the development of data capture and monitoring plans, reporting of Serious Adverse Events as they occur and completion of Food and Drug Administration (FDA) and sponsor forms in accordance with GCP timelines
  • Collaborates with primary investigator, sponsor and research staff to plan, conduct and evaluate project protocols, including research subject recruitment
  • Completes regulatory documents, data capture and monitoring plans
  • Assists with preparation for audits and response to audits
  • Provides and documents education as needed
  • Minimum two years clinical research or healthcare experience required
  • Bachelor's degree in healthcare or science field may offset experience requirement
  • Demonstrated basic computer proficiency
  • Strong organizational, communication and interpersonal skills
  • Must be self-directed with demonstrated ability to work independently yet establish cooperative relationships with colleagues
52

Research Coordinator Resume Examples & Samples

  • Collaborate with study personnel in the planning and submission of grant applications for internal and external funding
  • Integrate information from multiple sources to ensure that research proposals meet the necessary requirements of funding agencies
  • Conduct literature reviews on topics pertinent to research protocols and strategic initiatives
  • Design, create and revise data collection tools in collaboration with principal investigator, statistician and data management team, and conduct data entry as needed
  • Coordinate quantitative and qualitative data collection efforts for one or more research projects, which may include other collaborating agencies or institutions
  • Manage research participant contact and report problems and concerns to principal investigator
  • Manage project timelines and prepare interim reports for principal investigators, industry sponsors and institutional review board to ensure timely completion of each project
  • Liaison between the project team and funding agencies or significant parties
  • Reviews applications for research projects to ensure that protocols meet regulatory and ethical standards for the protection of human subjects
  • Provides consultation services and acts as liaison to DA2 investigators, staff and students, on the application and implementation of the federal regulations, state laws, and CHS institutional policies for human subject research
  • Maintains IRB records, both in paper and electronic format, submission of IRB applications, amendments, procedural changes, and continuing oversight of compliance
  • Prepares presentation materials and delivers educational programs on regulatory and ethical compliance in research to DA2 investigators, staff and students
53

Research Coordinator Resume Examples & Samples

  • Research study participant recruitment, screening and enrollment
  • Schedules patients' appointments and appropriate testing for patients as directed. Verifies information from patients including demographic and health insurance information
  • Follow-up in accordance with specific protocol
  • Reports to the principal investigator any deviations of normal operations
  • Reports to the principal investigator any unusual occurrences related to research study participants, staff or equipment
  • Reports immediately any changes in the research study participant's condition warranting intervention
  • Maintains appropriate communication with study sponsor and referring physicians
  • Responsible for preparation and submission of protocols for Research/Human Subjects Committee (IRB) approval. The scope of the clinical trials includes evaluation of therapy, assessment of effect of treatment, ongoing evaluation and long-term assessment of comprehensive management program, and evaluation of the effects of risk factor modification program
  • Responsible for completion of pertinent data relevant to patient enrollment in clinical research studies/clinical trials and management of data from procedures performed
  • Demonstrates knowledgeable assessment skills while constantly monitoring the patient's status throughout the duration of the clinical research study/clinical trial
  • Assists the principal investigator in the evaluation, care and follow-up of research study participants
  • Maintains appropriate study participant research records and documentation
  • Shall be accountable for maintaining the confidentiality and security of all medical center related, clinical trial related, medical staff related and patient related data and information as per HIPPA standards
  • Shall be accountable for abiding by all relevant policies and procedures
  • Responsible for maintaining annual competencies, training, and certifications as required
  • Performs other related duties as requested
  • Ability to read, speak, write, and understand the English language
  • Ability to complete mathematical computations required to perform tasks
  • Strong interpersonal, organizational, and oral communication skills
  • 2-3 years experience in a health care setting as a research coordinator or a comparable position
  • Experience with organization of medical charts preferred
  • Strong interpersonal and telephone skills required
  • Word-processing and computer data entry experience preferred
  • Typing skills must be a minimum of 30 wpm
54

Assistant Clinical Research Coordinator Resume Examples & Samples

  • Experience working in a Cancer Center and familiarity with members of Cancer Center team and patients
  • Familiarity with chart review and tracking relevant data from charts ; record data with extreme accuracy
  • Attention to detail and the ability to work effectively with a wide range of individuals and groups at all levels of authority
  • Experience with database software, MS Office
55

Market Research Coordinator Resume Examples & Samples

  • Facilitate departmental interactions with Procurement, including
  • Submit procurement requirements: Confidential Disclosure Agreements (CDAs), requisitions, and bid exceptions
  • Track requisition approval status, assignment of Purchase Orders (POs), and invoice payments
  • Track spend vs. budget for overall department as well as individual molecules and indications
  • Track secondary/syndicated subscriptions, user credentials, and renewal dates
  • Coordinate vendor site visits: introductions, capabilities meetings, and evaluations
  • Coordinate SurveyMonkey-type activities – documenting objectives and key questions, creating and fielding surveys, and summary of results, as needed
  • Ensure the following materials are posted to SharePoint in a timely manner: final project reports, relevant vendor contact info and capabilities presentations, team member status reports, and other materials, as needed
  • Process expense reports, as needed
  • Disseminate research travel logistics to attendees (dates, facility locations, and recommended hotels)
  • Maintain master department calendar and non-Regeneron partner contact list
  • Book internal and external meetings, including meeting invites, conference rooms, catering, directions, and security registration, as needed
  • Coordinate departmental staff meetings and communicate action items, next steps, and new topics
  • Coordinate internal collaboration meetings across Commercial and non-Commercial teams
  • Consistent coordination and communication with Commercial staff regarding workload balance and coverage, facilities needs and issues, and companywide activities
  • Basic administrative assistance as needed, including: management of travel needs, copying and printing of materials, coordination with shipping and receiving, presentation support
56

Assistant Clinical Research Coordinator Resume Examples & Samples

  • Familiar with excel
  • Ability to navigate web based databases
  • Strong interpersonal and organizational skills desired
57

Research Coordinator Resume Examples & Samples

  • Degree in business administration or related field
  • Proficiency in the use of MS Word, Excel, PowerPoint, Outlook. Experience with both Macintosh and Windows platforms a plus
  • Demonstrated ability to communicate with university students, faculty, administration, community program participants, community partners
58

Research Coordinator Resume Examples & Samples

  • Coordinates day to day activities of clinical research protocols
  • Ensures accurate data collection, documentation, organization and safety of study volunteers
  • Required: Three Years of relevant experience in a research setting without a Bachelor degree
  • No experience required if candidate has a Bachelor degree in a related field
59

Research Coordinator Resume Examples & Samples

  • Self-directed, independent and organized
  • Requires experience using Excel and knowledge of database management
  • Requires the ability to understand and implement patient studies and protocols
  • Prefer experience with specimen handling
  • Bilingual a plus
60

Research Coordinator Resume Examples & Samples

  • Responsible for recruiting, advertising, and screening for research participants. This involves identifying advanced cancer patients from the institutional database, coordinating with physician collaborators to contact patients and their family caregivers in the clinic for the purpose of recruitment, and registering study participants on the protocol. Recruitment may be exclusively at Baylor Clinic other sites in the Texas Medical Center depending on project needs
  • Collects and enters data into study databases
  • Supervision: Not normally required to supervise others
  • Customer Service: Takes routine or required customer actions to meet customers' needs. Responds promptly and accurately to customers' complaints, inquiries, and requests for information and coordinates appropriate follow up
  • Working Conditions: Generally, work is done in an office environment with pleasant working conditions. There is good lighting and ventilation, it is reasonably quiet, and the work hours are reasonably regular
  • Physical Requirements: Rarely required to exert physical effort
  • Physical Risk: Does not handle/work with biohazards or risks for potential job-related injuries
  • Required: One year of relevant experience in a research setting with Bachelor degree or Five years of relevant experience in a research setting without a Bachelor degree
61

Research Coordinator Resume Examples & Samples

  • Collect and document research data
  • Maintain records for clinical study and regulatory documents
  • Enter data into a computerized database or case report forms
  • May schedule research subject appointments for tests and procedures, such as laboratory tests for the research protocol
  • Retrieve and submit test results to appropriate party
  • May obtain specimens
  • Ship specimens
  • Correspond with patient throughout study
  • Order supplies and equipment
  • Work with multiple hospital information systems such as the VA EMR, EPIC, BRAIN and Access and Excel databases
  • Organize research protocols as designated by specific protocol guidelines and report to principle investigator
  • Perform other job related duties as assigned, including writing and reviewing drafts of manuscripts
  • Preferred: Masters in Public Health
  • Experience Required: Two years of relevant experience in a research setting with Bachelor degree or Six years of relevant experience in a research setting without a Bachelor degree
62

Assistant Clinical Research Coordinator Resume Examples & Samples

  • Excellent leadership and organizational skills with high attention to detail
  • Experience with and familiarity with Autism and Learning Disabilities resources in the Bay Area
  • Experience with recruitment of research participants for clinical studies, including contacting and visiting schools, working with children and adolescents in experimental settings, working with diverse populations, clinical interviewing and community outreach
63

Research Coordinator Resume Examples & Samples

  • Recruit, advertise, and screen for research patients
  • Conduct patient interviews to evaluate patient eligibility in the study
  • Schedule research subject appointments for tests and procedures, such as laboratory tests, x-rays, and other studies specific for the research protocol
  • Retrieves and submits test results to the appropriate party
  • Correspond with the patient throughout the study
64

Senior Research Coordinator Resume Examples & Samples

  • Required: Bachelor's degree in a related field; four years of relevant work related experience in a research setting can be substituted in lieu of a degree
  • Required: Five years of relevant experience in a research setting with Bachelor's degree or nine years of relevant experience in a research setting without a Bachelor's degree
  • Certified Clinical Research Coordinator (CCRC) or Certified Clinical Research Professional (CCRP) preferred
  • Bilingual, English and Spanish, is a plus and preferred
65

Senior Research Coordinator Resume Examples & Samples

  • Phlebotomy experience preferred
  • Bilingual, English and Spanish, is preferred but not required
  • Ability to communicate with patients, families, doctors, and other healthcare providers
  • An in-depth working knowledge of IRB requirements, FDA regulations, Good Clinical Practice, and ICH guidelines for the conduct of clinical trials
  • Must be conscientious, detail-oriented and be able to effectively manage multiple priorities concurrently
  • Coordinate and establish priorities among diverse tasks
  • Proper utilization of medical equipment and supplies and experience with specimen processing
66

Research Coordinator Resume Examples & Samples

  • Preparing policy briefs and summaries relating to short term rental legislation to present internally to staff
  • Daily monitoring of municipalities relating to relevant regulatory events
  • Short and long term tracking of local city governments current and future regulations
  • Providing comprehensive policy analysis on regulatory issues in markets including city codes, staff reports, and policy discussions
  • Meeting with regional policy managers and outside consultants to liaison with the San Francisco research team
  • Track and compile relevant press on short term rental regulations and legislation
  • Maintains a number of documents and internal processes relating to the ongoing legislative status and regulatory details to policy leads
  • Supports comprehensive tracking and reporting systems for each project, and , update and organize shared drives/files
  • Build relationships and working with cross-functional teams
  • Assist with other assignments and tasks as necessary
  • A bachelor's degree or from an accredited four-year institution
  • Exhibit strong process-oriented skills and strive to find the most efficient way to do things without sacrificing a high quality of work and/or results
  • Strong work ethic, and exhibit professionalism, courtesy and strong interpersonal skills
  • Ability to exercise judgment and maintain confidentiality
  • Demonstrate outstanding pro-active and multi-tasking abilities
  • Acute attention to detail and follow through, and are very organized
  • Ability to work effectively on multiple projects at once and meet deadlines
  • Excellent research, writing, and verbal communication skills related to public policy and legislation
  • Understanding of local city government structure and process
67

Research Coordinator Resume Examples & Samples

  • Graduate degree in economics, public policy, social work, or a closely-related field
  • Experience with navigating University of Washington and/or Washington State Institutional Review Board research procedures
  • Experience with using or analyzing administrative or complex longitudinal data
  • Social science research experience, particularly on politically salient issues related to labor market inequality such as the minimum wage
  • Mixed-method research interest or experience
68

Research Coordinator Resume Examples & Samples

  • Manage day-to-day operations of specific projects including logistics, scheduling, resource/equipment planning, staffing
  • Work with subject matter experts to enable process for improving and expanding conventions for analyst workflows
  • Manage collection of project-specific data
  • Own the logistics and reporting for these collections
  • Communicate directly with participants, tracking and responding to written requests and in-person as needed
  • Lead small to medium projects related to improving existing processes or launching new projects
  • Partner closely with Program Managers and team members on protocol/process development for existing and future collections
  • Continuously evaluate data collection tools and processes and offer solutions to ensure they are efficient, high quality, and scalable
  • Bachelor’s degree in a relevant field (including, but not limited to, Linguistics, Sociolinguistics, or Communications)
  • Excellent proficiency in US English and familiarity with language use specific to the United States culture
  • Detail-oriented, with experience balancing multiple tasks and deadlines
  • Ability to distill complex concepts into clear written guidelines
  • Experience working with various internal teams (including technical) to execute on requirements, surface and mitigate risks to delivery, and develop processes and tools
  • Experience with data collection, processing, throughput analysis & reporting
  • Excellent ability and methodology to troubleshoot and identify the root cause of issues
  • Dedicated, self-motivated and dependable
  • Willingness to support several projects at one time, and to accept reprioritization as necessary and to deliver high-quality work on schedule
  • Willingness to learn new processes and tasks in a growing and changing environment
  • Experience in understanding metrics and developing them, as required
  • Background in linguistics or experience with language processing, transcription, or annotation
  • Experience with Linux, query languages, and scripting languages
69

Research Coordinator Resume Examples & Samples

  • Creation of KTAZ, KHRR, KBLR & KDEN daily success stories and distribution of daily overnights
  • Assist in maintaining Arianna (overnight ratings program) and pull special trend reports as needed
  • Maintain Nielsen Enames module to ensure proper programming measurement
  • Create and design rating highlights sheets from both NSI and NSI-H during each sweep period
  • Assist in rating estimates for new programs for KTAZ, KHRR, KBLR & KDEN, along with analyzing competitive programming
  • Put together sales presentations and media kits as needed by staff
  • Help maintain and post information to the NBCU Portal
  • Assist Director on special research projects and analyses
  • Minimum one year TV research, media or agency experience
  • Willingness to travel, work overtime and on weekends with short notice as necessary
  • Must be willing to work at the station in Phoenix location
  • Must be 18 years or older
  • Must be covered by Solutions, NBCU’s Alternative Dispute Resolution Program
  • Demonstrated expertise using Microsoft Office applications including Excel, PowerPoint and Word
  • Bilingual preferred, but not required
70

Oncology Clinical Research Coordinator Resume Examples & Samples

  • Understands medical terminology
  • Demonstrates appropriate phone skills and effective use of the computer
  • Minimum two years of health care experience in ambulatory or acute care setting, Clinical Research experience preferred
  • Currently holds a Nebraska Medication Aide Registration if not a licensed medical provider or willing to acquire within one month of employment
  • Demonstrated knowledge of the clinical trial process and the Federal regulations that govern the conduct of clinical trials preferred
71

Research Coordinator Resume Examples & Samples

  • Processes research applications submitted to the hospital for review and approval
  • Reviews applications for completeness, contacts PI and/or study sponsors with hospital-related questions, works with PI and study coordinators to facilitate completed applications and review
  • Discusses/reports findings with Director of Revenue Analysis or Designee
72

Oncology Clinical Research Coordinator Resume Examples & Samples

  • Coordinates the initiation and activation of all new clinical trial protocols. This includes, but is not limited to, verifying Scientific Review Board (SRB), Institutional Review Board (IRB), Human Research Oversight Committee (HROC), data collection plans and finance/contract approvals prior to study activation. Coordinates the preparation of study tools including but not limited to study binders, medication diaries, eligibility checklists and flow sheets (as required)
  • Using Oncore®/Excel ®/Word, develops study tools, including but not limited to eligibility checklists, medication diaries, calendars, and flow sheets (as required)
  • In collaboration with the Research Nurse Clinician (RNC) and/or physician, reviews patients’ charts and medical history to confirm protocol eligibility and obtains source documents (i.e. medical record documentation) as needed. Under the direction of the RNC and/or physician, ensures that IRB approved informed consent form has been obtained, signed, placed in the medical record, and that a copy was provided to the patient
  • Registers consented research patients with study sponsor (e.g. industry, NCI Cooperative group, etc.) and inputs into Oncore® clinical trials database maintained by Cancer Institute of New Jersey
  • Maintains research record (e.g. patient consent, eligibility, Case Report Forms (CRF), registration confirmation, corresponding source documents, etc.) for all patients enrolled in Cancer Institute of New Jersey clinical trials. This includes, but is not limited to, Cancer Institute of New Jersey Network centers (Cancer Institute of New Jersey investigator-initiated trials), community physicians’ offices and hospitals
  • In collaboration with the RNC and physician, assists with grading adverse events using the most recent version of National Cancer Institute (NCI) common toxicity criteria or protocol specific grading scales. Completes Serious/Unexpected Adverse Event (SAE) form for all internal and multicenter serious/unexpected adverse events as required by study sponsors, federal requirements and institutional guidelines
  • Ensures research record (e.g. patient consent, eligibility, CRFs, registration confirmation, corresponding source documents, etc.) is maintained for all patients enrolled in Cancer Institute of New Jersey clinical trials. This includes, but is not limited to, Cancer Institute of New Jersey Network centers (Cancer Institute of New Jersey investigator initiated trials), community physicians’ offices and hospitals
  • Using Oncore®, provides regular reports to the tumor study group members and Principal Investigator on all studies to which he/she is assigned
  • Understands and anticipates needs of study sponsors. Serves as study liaison with study sponsors, schedules monitoring visits and conference calls. Provides accurate, timely, intelligent responses to sponsors’ queries
  • In collaboration with the RNC, assures that Cancer Institute of New Jersey personnel, including investigators, are conducting the study according to the treatment plan and GCP guidelines
  • Actively participates in weekly tumor study group meetings and conference calls (if applicable)
  • Actively participates in ongoing research specific quality assurance activities such as chart audits for protocol compliance
  • Communicates effectively with staff and outside agencies, and assists in the promotion of teamwork, contributes to OHRS espirit de corps
  • In collaboration with Tissue Analytical Services (TAS), ensures study specific deadlines are adhered to including the submission of pathology materials, serum, blood, urine and tissues samples, and CRFs
  • Collaborates with TAS and/or OCRC I/II staff members, to ensure procurement of protocol specific bio-specimens (e.g. blood, urine and tissue) are collected and processed according to protocol specific guidelines
  • Obtains and submits x-rays, pathology reports and any other specialized reports as needed
  • Maintains up-to-date knowledge and adheres to policies and procedures set forth by RBHS, Cancer Institute of New Jersey, FDA, and all regulatory bodies. Documents and maintains mandatory RBHS employee requirements such as Blood Borne Pathogens, Right-to-Know, Tuberculosis, Hand-Washing, as defined by Environmental & Occupational Health & Safety Services (EOHSS), Joint Commission on the Accreditation of Healthcare Organizations (JCAHO) and other institutional requirements
73

Research Coordinator Resume Examples & Samples

  • Relevant experience in clinical research with a strong cardiovascular knowledge base
  • Clinical cath lab experience preferred
  • Must have flexibility in hours based on needs of position including potential for off-hour need
  • Ability to effectively solve problems, balance multiple priorities and handle confidential issues
  • Thorough knowledge of federal and institutional policies governing clinical research required. Knowledge and experience of regulatory guidelines, FDA policies, and IRB guidelines a must
  • Proficiency with PCs and windows-based software, including Word and Excel, Microsoft Access
74

Clinical Research Coordinator, Senior Resume Examples & Samples

  • Bachelor’s degree in a field appropriate to the area of assignment AND four years of research administrative/coordinative program experience; OR, Master’s degree in field appropriate to area of assignment AND three years of research administrative/coordinative program experience; OR, eight years of progressively responsible research administrative/ coordinative program experience; OR, any equivalent combination of experience, training and/or education
  • Previous human subjects training (e.g. CITI certification) and four years experience as a research coordinator and/or research specialist senior conducting clinical research, and data analysis and reporting
  • Ability to follow strict protocols and standard operating procedures
  • Previous supervisory and training experience
75

Senior Clinical Research Coordinator Resume Examples & Samples

  • Serve as a resource to others for all aspects of conducting a complex and multi-site clinical study
  • Develop and implement plans and standard operating procedures under the guidance of study leadership
  • Collaborate effectively with others to ensure proper progress and completion of studies
  • Supervise activities of subordinates, if assigned
  • Train new staff in preparation and conduct of clinical trials
  • Provide oversight and guidance as needed to research staff
  • Collect and process specimens to meet study requirements, including saliva specimens and intravenous blood samples
  • Coordinate and participate in monitor visits, audits, and quality reviews (internal and external) in a professional manner
  • Prepare study staff and participate directly in recruitment/enrollment
  • Create and maintain a detailed tracking system for participants considered for enrollment. Track progress at regular intervals and report out to PI and study team
  • Proactively take initiative to ensure recruitment stays on track with the project timelines
  • Communicate study-related issues to investigators, sponsors, coordinating centers, study coordinators, clinical team, managers and other institutions in a timely fashion
  • Oversee data entry and validation to ensure accuracy, quality and compliance of data collection process
  • Ensure quality of data submitted from study sites and assure timely submission of data
  • Assist other members by educating, providing resources and consulting on difficult protocols or projects
  • Master’s degree in a field appropriate to the area of assignment AND three years related research experience; OR, Bachelor’s degree in a field appropriate to the area of assignment and four years related research experience; OR, Any equivalent combination of experience, training and/or education approved by Human Resources
  • Bilingual highly preferred (Spanish, Navajo/Diné Bazaad, other)
  • Previous supervisory experience
76

Research Coordinator Resume Examples & Samples

  • Bilingual (English/Spanish) preferred
  • Requires effective communication skills, both orally and in writing
  • Experience with computer spreadsheets and database management
  • Ability to understand and implement patient studies and protocols
  • Must have interpersonal skills necessary to coordinate research studies
77

Research Coordinator Resume Examples & Samples

  • Assists in developing research plans and project designs
  • Screens and schedules research participants
  • Coordinates protocol activities and works with research participants in accordance with human subjects requirements
  • Administers questionnaires and testing procedures
  • Collects, manages, and tabulates research data and ensures its accuracy and security
  • Assists in preparing project reports and manuscripts; processing regulatory documentation for submission
  • May also assist with coordination of some administrative duties, including keeping track of grant budgets and regulatory schedules; organizing meetings; and purchasing and replenishing of supplies
78

Research Coordinator Resume Examples & Samples

  • Analysis
  • Budget development and control
  • Organization
79

Senior Clinical Research Coordinator Resume Examples & Samples

  • Assist in planning and implementing the clinical study's goals and objectives; organize patient enrollment planning; conduct quality assurance activities, compile and analyze data
  • Develop and implement procedures, maintain records, track progress, and conduct quality assurance on data collected
  • Prepare, submit, and assist Director with multiple levels of research documentation (i.e. IRB submissions, educational materials, reports, grant renewal reports, and study forms)
  • Act as a liaison with medical staff, University Departments, ancillary departments and/or satellite facilities
  • Provide direct supervision to non-exempt staff (i.e. hiring/firing, performance evaluations, disciplinary actions, approve time off, etc.)
  • Maintain regulatory documentation
  • Perform related duties including level1 duties based on departmental need
80

Research Coordinator Resume Examples & Samples

  • Three years of grant management experience is required. Preference for that experience to have been in an academic environment
  • The ability to manage competing deadlines and be responsive to the needs of multiple PIs and departments
  • Demonstrable working knowledge of the OMB Uniform Guidance
  • Advanced experience with Excel
81

Senior Clinical Research Coordinator Resume Examples & Samples

  • Provide direct supervision to non-exempt staff (i.e. hiring/firing, performance evaluations, disciplinary
  • Bachelor’s degree in health-related field or equivalent experience
  • 2-5 years relevant experience
82

Research Coordinator Resume Examples & Samples

  • Demonstrated ability to juggle and drive multiple responsibilities for self, peers, and superiors
  • Excellent writing skills and attention to detail
  • Excellent time management, interpersonal, and written and oral communication skills
  • Candidates must exercise good judgment and be able to work independently with minimal direction and as part of a team
  • Advanced skills managing databases (including Excel) and preparing charts/graphs from data
  • Experience with research methodology, interest in both qualitative and quantitative data. Following coursework is desired: corporate finance, managerial accounting, and business statistics
  • Strong technical skills, ability to efficiently use computer software and tools to complete analysis or communicate work. Facility and creativity with communication technologies
  • Positive attitude and strong interpersonal skills that enable working as an effective member on a small team
  • Commitment to CRPE’s mission and interest in the work of the Center
  • Experience with statistical software especially R, presenting data, and preparing reports
  • Experience working with fiscal and education data
  • Master's degree in a social science-related field
  • Coursework in corporate finance, managerial accounting, business statistics
83

Research Coordinator Resume Examples & Samples

  • Coordinates and assures integrity of all activities associated with conducting a clinical trial as it relates to compliance with local, state, and/or federal regulatory requirements
  • Assists Principal Investigators in the preparation and submission of clinical protocols, consent forms, and other documents to the scientific review committee, IRB and other regulatory organizations
  • Maintains regulatory files related to DVBIC clinical investigations
  • Communicates with research participants, staff, regulatory affairs and data management groups, laboratory and clinical investigators, management, and outside collaborators
  • Recruits, interviews, examines, counsels, and educates clinical trial volunteers, administer and obtain informed consent
  • May collect and analyze data to evaluate volunteer eligibility for enrollment
  • May collect, analyze and interpret laboratory and clinical data obtained during a medical evaluation, report significant values, findings, and events that require prompt attention to clinical investigators
  • Assists with the documentation and reporting of adverse events, completes and reviews Case Report Forms for patient eligibility, protocol compliance, omissions, errors, and submits these forms as required
  • Prepares and maintains written and electronic volunteer databases/logs
  • Perform data extraction and chart reviews of patients’ medical records
  • Reviews the source document file for information such as verification of critical variables, entrance criteria, visit date, and lab data
  • Ensures that research records are stored and secured properly, and that inventory and records are updated and properly maintained
  • Conducts data verification as indicated, documents, assists the investigator and protocol coordinator with questions, may transcribe and resolve queries of data in case report forms (hardcopy or electronic)
  • Prepares documents, under direction of project leads
  • Reports statistical analyses and descriptive data from patient's study books to be used in research reports
84

Clinical Research Coordinator, Senior Resume Examples & Samples

  • Eight (8) years equivalent combination of experience, training and/or education approved by Human Resources; OR
  • Bachelor’s degree in a field appropriate to the area of assignment and four years related research experience; OR,
  • Master’s degree in a field appropriate to the area of assignment AND three years related research experience
85

Research Coordinator Resume Examples & Samples

  • 1-2 years of work experience, preferable in the broadcast media industry
  • Advanced skills utilizing Microsoft Excel and proficient in Microsoft Outlook Word, PowerPoint and Access
  • Dynamic, flexible, hard-working and highly organized
  • Superior interpersonal skills
  • Detail oriented with strong analytical and research skills
  • Familiar with Nielsen ratings, MRI, comScore & Media Math preferred
86

Research Coordinator Resume Examples & Samples

  • Conduct research literature searches and summarize findings in an organized format
  • Collect and manage survey data, download data from diabetes management devices, and complete electronic medical record reviews
  • Meet with families in busy outpatient and inpatient medical settings
  • Develop and maintain databases in Microsoft Excel and statistical software packages (SAS, SPSS, etc.)
  • Complete all required training modules related to the Responsible Conduct of Research (e.g., CITI Program training)
  • Evening and weekend telephone calls or meetings with study participants may be needed on occasion
  • Learning about type 1 diabetes by observing patient/family diabetes education classes and/or medical visits at the Texas Children’s Hospital (TCH) Diabetes Care Center, and completing readings and tutorials with the Principal Investigator and other diabetes experts at TCH
  • Learning to use the TCH electronic medical record, EPIC, to identify and track patients with diabetes
  • Learning how to recruit and enroll eligible families, and to obtain informed consent for behavioral research
  • Learning to collect and manage data from quantitative questionnaires, diabetes-related technologies such as blood glucose meters, and electronic medical records
  • Learning to complete required compliance-related documentation for behavioral research
  • Learning to develop an organizational system for managing all aspects of study implementation (e.g., participant incentives, study visit scheduling, medical chart reviews)
  • Learning to work independently and as part of a larger study team
  • Prior experience with Microsoft Excel and SPSS or SAS (statistical software programs) is required
  • Previous experience interacting with children and families and/or experience in health care settings is required
  • Experience with culturally diverse children and families is preferred
  • The individual is expected to be highly organized, keep detailed records, and display good verbal, communication, and problem-solving skills
  • Respectful, patient-centered interactions with participants, medical providers, and staff are expected at all times
  • Study activities will largely take place at three TCH/BCM locations in the Houston metro area: West Campus (Katy), The Woodlands, and Texas Medical Center. The candidate must be able to travel between those locations. Mileage for travel between locations and parking expenses will be reimbursed
  • Work is located in busy patient clinics, hospitals, office areas, and/or laboratories where there are potential exposures to blood borne pathogens (blood &/or other potentially infectious materials), drugs, chemicals, radiation, and physical hazards. Patient interaction and interaction with other employees is required
87

Research Coordinator Resume Examples & Samples

  • Organizes research protocols as designated by specific protocol guidelines
  • Conducts all testing procedures required by study protocol
  • Evaluates and analyzes clinical research data
  • Prepares documentation necessary to obtain initial and continued approval for the specific research protocol
  • Two years of relevant experience in a research setting with Bachelor degree or Six years of relevant experience in a research setting without a Bachelor degree
88

Research Coordinator Resume Examples & Samples

  • Oversees the organization and compliant execution of research projects with the proper allocation of resources and adherence to research protocol requirements
  • Oversees compliant research program operations and finances of assigned area(s)
  • Participates in process improvement activities
  • Potentially assists PI with research study design and development of research protocol
  • Supervises and coordinates research project budget development
  • Potentially negotiates industry-sponsored research budgets. Supervises research subject recruitment and data management
  • Minimum five years clinical research experience, including prior work lead and coaching experience
  • Advanced degree in health care, science or business may offset some of the experience requirement
  • Requires knowledge of budgeting, cost analysis, manpower planning, supervision and operational analysis
  • Demonstrates basic computer proficiency. Strong organizational, communication, interpersonal and analytical skills
  • Must be self-directed with demonstrated ability to work independently, yet establish cooperative relationships with colleagues
89

Research Coordinator Resume Examples & Samples

  • Bachelor's Degree in a related science or engineering field
  • Interest in, and knowledge of, energy-related technologies
  • Excellent written and verbal communication skills with the ability to convey scientific knowledge across technical and general populations
  • Excellent interpersonal skills, including the ability to interact with a diverse population comprising Princeton University community members, corporate executives, funding agency representatives, and external administrative staff
  • General knowledge of university research activities and sponsored research principles
90

Research Coordinator Resume Examples & Samples

  • Serves as primary study coordinator for research protocols in the outpatient clinic or at affiliated hospital as assigned by the Director
  • Directs the conduct of clinical studies to ensure adherence to the research protocol
  • Screens patient records, databases and physician referrals for identification of prospective candidates for research protocols
  • Interviews prospective subjects for participation in investigations and obtains informed consent
  • Participates in initiation visits/investigator meetings for assigned clinical trials (may involve travel) and implements these trials according to a deadline schedule mutually agreed upon by PI and sponsor
  • Educates human subjects for participation in investigations
  • Educates clinic/hospital personnel for participation in protocol conduct, data collection process and related issues as applicable
  • Ensures all study personnel have completed required training and training is documented, before conducting protocol related activities
  • Maintains consistent enrollment in protocols and provides monthly, written documentation of screening/enrollment/follow-up activities
  • Draws, processes,prepares and ships laboratory samples for clinical trials
  • Performs ECG’s, Holter monitoring and other procedures as directed by study protocol
  • Instructs Principal Investigator on procedures and tests that need to be performed in compliance with the study protocol and advises PI on the results of procedures and testing; calling to attention findings of clinical importance
  • Documents research related examinations, procedures, tests and other activities in appropriate clinic or hospital charts
  • Document phone conversations with sponsors, study subjects, physicians and coordinating organizations
  • Schedules follow-up visits for study subjects with appropriate personnel in and provides source documentation for activities conducted during these visits
  • Completes accurate and complete data entry into case report forms or pre-established computer programmed formats
  • Schedules and undergoes Coordinates and participates insponsor initiated monitor visits and quality assurance audits for periodic reviewing and querying of collected data in a timely manner
  • Identifies strategies to improve patient enrollment in research protocols in collaboration with the PI
  • Report all serious or unexpected adverse events immediately to physician or Research Director, maintains documentation and review of AE’s
  • Assist in reporting all serious or unexpected adverse events to appropriate regulatory agencies (sponsor, IRB) in a timely manner
  • Assists in maintenance of patient flow sheets and research data base
  • Acts in accordance with The Practices principles and practices
  • Performs delegated duties as assigned
91

Research Coordinator Resume Examples & Samples

  • Bachelor's Degree in a related field; four years of relevant work related experience in a research setting can be substituted in lieu of a degree
  • Experience using Electronic Medical Record Systems
  • Fully fluent in English and Spanish
  • Ability to tend to details
  • Ability to maintain confidentiality of patient information to include protected health information
  • Ability to communicate with patients in a compassionate, non- judgmental manner
92

Clinical Research Coordinator, Senior Resume Examples & Samples

  • Oversee the team of Clinical Research Nurses, Coordinators, and Cord Blood Collectors at CCBB staffed collection sites
  • Develop Team leads as mid-level managers
  • Coach, mentor and motivate team members
  • Perform all personnel actions, including interviewing, hiring, and performance management
  • Develop and strengthen current communication channels to allow for sharing of best practices across sites
  • Visit collection sites regularly
  • Ensure that scheduling coverage for collections at all hospital sites is complete for each month
  • Set goals for collection sites
  • With the assistance of the Marketing Manager, the Education Specialist and the Collection Sites Team Leads, develop and implement incentive programs to increase the number of banked cord blood units and to increase participation of hospital medical staff
  • Identify and share best practices across sites
  • In conjunction with Marketing Manager, Education Specialist and Collection Sites Team Leads, develop and oversee implementation of continuous improvement strategies for staffed, hybrid and kit sites
  • Work closely with the Marketing Manager and the Education Specialist to develop programs with the goal of promoting the Carolinas Cord Blood Bank and to develop education tools that promote public awareness of cord blood banking the community
  • Present to community groups as needed to increase awareness of cord blood banking
  • Represent the Medical Director in interactions with hospital staff, on national and international cord blood collection committees, and at outside meetings and conferences
  • Maintain liaison with hosting hospital managers and staff to solve operating problems that may arise at any one of CCBB's collection sites
  • Ensure good relationships with staff at CCBB's hybrid sites is maintained and strengthened
  • Work closely with CCBB Marketing Manager to provide regular updates to hospital staff and collection overview for directors, doctors and staff from affiliated sites and to develop educational tools that promote public awareness of cord blood banking in the community
  • Collaborate with Collections Logistics Manager on the development and modification of standard operating procedures (SOPs) related to collection of cord blood
  • Work closely with QSU staff, the Collection Logistics Manager and the Training Coordinator to prepare training materials for new and updated operating procedures
  • Represent collections at outside and internal audits including FACT, FDA and QSU
  • Completion of an Associates degree plus a minimum of six years of research experience, or
  • Completion of a Master's degree and a minimum of 2 years of research experience
93

Senior Clinical Research Coordinator Resume Examples & Samples

  • Helping with patient enrollement and patient interaction
  • Working with site budgets
  • Ensuring regulatory documents are in place
  • Responsble for managing any new CRC hires
  • Management over 3 clinical staff
94

Research Coordinator Resume Examples & Samples

  • Serve as the Executive Assistant to the Executive Vice President, Research: plan meetings, route phone calls, edit power points, and manage calendars
  • Track and ensure delivery of acquisition scripts and screeners; distribute materials and assignment information to contractors and staff
  • Research and write due diligence reports for National Geographic Partners
  • Write quick passes for acquisitions
  • Quality Check shows which have completed research process
  • Track contractor expenses and payments, and process invoices
  • Consistent maintenance of department project database (FILEMAKER) including support for remote users
  • At least 1 year of research experience in an academic or professional context
  • Proficient in Microsoft Office. Experience in FILEMAKER and VPS is a plus
  • Proficient is Spanish is a plus
95

Lead Clinical Research Coordinator Resume Examples & Samples

  • Train new and current Clinical Research Coordinators and Research Assistants to ensure effective coordination of training activities in the clinical trials processes
  • Assist CRC’s and RA’s with assigned tasks as necessary
  • Provide clinical support and assistance in the assignment of CRC’s, Raters, and other staff
  • Troubleshoot and resolve clinic, protocol, and SOP issues and advise CRC’s
  • Assist coordinators with assigned tasks as necessary
  • Problem solve protocol issues with staff as necessary
  • Work closely with the Research Manager to improve and streamline clinic processes
  • Assist the Research Manager with projects and tasks as assigned
  • Fill in as needed in the absence of CRC’s
  • Acting Supervisor or point of contact in the absence of the Research Manager
  • Resolve problems quickly + in a positive manner
  • Minimum of 2 years of clinical research experience required; CCRC strongly preferred
96

Research Coordinator Resume Examples & Samples

  • Collaborates with primary investigator, sponsor and research staff to plan, conduct and evaluate project protocols
  • Assists with the recruitment, selection and monitoring of research project participants
  • Manages the handling of adverse events, compliance and other participant-related issues
  • Minimum two years prior clinical research or health care experience required
  • Bachelor's Degree in a health care or science field can substitute for years experience
97

Senior Clinical Research Coordinator Resume Examples & Samples

  • Data entry for clinical research projects including but not limited to
  • Entry of clinical data from test requisition forms
  • Entry of clinical data from medical record forms
  • Entry of clinical data from phone interview
  • Email/Phone follow-up for research projects as directed by supervisor or supervisor’s designee
  • Data queries development and execution as needed
  • Data analysis as directed by supervisor or supervisor’s designee
  • Literature review related current and active research projects
  • Other tasks to assist with current research, variant assessment/reporting or marketing group projects as directed by supervisor or supervisor’s designee
  • Occasional coverage for clinical assistants as needed
98

Research Coordinator Resume Examples & Samples

  • 3 years working with American Indian communities
  • 2 years of experience as a Project Coordinator or similar
  • 5 years working with American Indian communities
99

Senior Research Coordinator Resume Examples & Samples

  • Coordinates and ensures accurate protocol implementation and conduct for all assigned protocols
  • Coordinates regulatory and IRB interactions in collaboration with the ICTR regulatory staff. ? Recruits, screens, and enrolls research participants
  • Assists Principal Investigator with informed consent
  • Coordinates care for research participants enrolled on assigned protocols to ensure that the study is implemented as it is written and that all required data are available and collected
  • May collect, process and ship laboratory specimens
  • Performs patient/family education about clinical trials as well as the research protocols
  • Ensures research needs are met at all family meetings (discuss progress of treatment, changes in therapy)
  • Acts as liaison between patient and physician concerning problems, adverse reactions, and other patient care issues, that may be related to the study. Follows-up with patients during each clinic visit to answer questions and assess for toxicities
  • Coordinates affiliate involvement with study conduct, Investigational Pharmacy, Research Office, Diagnostics, Credentialing, etc., as needed
  • Five years of relevant experience in a research setting with a Bachelor's degree or nine years of relevant experience in a research setting without a Bachelor's degree
100

Senior Clinical Research Coordinator Resume Examples & Samples

  • Provide oversight for the preparation, review, submission and maintenance of regulatory activities/submissions within our team to the national IRB; ensure accuracy and timeliness of distributing regulatory updates to all collaborative parties
  • Bachelor’s degree in a field appropriate to the area of assignment and four years related research experience; OR, Master’s degree in a field appropriate to the area of assignment AND three years related research experience; OR, Any equivalent combination of experience, training and/or education approved by Human Resources
  • Bilingual (Spanish, Navajo/Diné Bazaad, other)
101

Senior Research Coordinator Resume Examples & Samples

  • Manage qualitative workflows and pipelines from across the network
  • Work with internal and external departments to understand research objectives
  • Develop and program recruitment screener to target specific audience groups per client need, for applicable qualitative projects
  • For applicable qualitative projects, develop facilitation guides and/or community engagement tasks
  • Oversee and manage vendors for execution of online work as well as moderate members of community sites to ensure quality research feedback
  • Manage scheduling and booking of focus group facilities, online platform vendors and respondent incentives
  • Assist with the development of analysis in various formats such as tab plans, graphs, memos, written report summaries, and/or efficient visual ways of understanding the data
  • Weekend and non-traditional business hours maybe required for this very fast paced role
  • Minimum of 3 years proven research experience, with at least 2 years in Qualitative research
  • Experience with both in-person and online moderation
  • Must have an understanding of general research processes and research design of qualitative research techniques
  • Solid grasp of traditional media research tools and social media platforms
102

UX Research Coordinator Resume Examples & Samples

  • Manage research projects across a variety of methodologies
  • Conduct qualitative studies (usability studies, click-tests, etc.), analyze data, share findings
  • Field surveys, analyze responses, and report findings
  • Maintain ongoing research initiatives including projects with external research vendors
  • Work cross-functionally with design, product marketing, and product management
103

Research Coordinator Resume Examples & Samples

  • Work with research consultants to identify and screen candidates, communicate with internal relationship representatives, manage and track approvals, outreach to participants, and coordinate scheduling
  • Establish user criteria and develop SQL statements to pull data from various databases
  • Partner and coordinate with individuals who have access to customers
  • Maintain participant lists for multiple studies
  • Build a database of participants that is continuously maintained and updated
  • Establish innovative and efficient ways to attract participants that comply with internal regulations regarding customer contact and communication
  • Screen participants for usability tests by interviewing participants over the phone and distributing/managing questionnaires. Manage, track, distribute and store participation incentives, NDA's and thank you gifts
  • Logistics such as schedule sessions, maintain calendars, schedule conference rooms, confirm with participants and other tasks for both remote and field research
  • Proactively communicate status updates and changes that impact ongoing research
  • Maintain and update SharePoint User Experience Research site - includes keeping Research Library up to date with all final reports, maintaining upcoming research calendar, ensuring that UxR marketing content is current
  • Manage research booth at Global Payment Conferences
  • Exemplary business communication and networking capabilities; ability to assess project issues early, and communicate appropriately to help manage expectations
  • Project management: ability to "juggle" time and effort across multiple projects and proven ability to deliver results within a specified time
  • Creative problem solving skills - filling research quotas is like putting together a puzzle and the successful coordinator will be someone who likes to work on a problem until it is solved
  • Exemplary organizational skills and penchant for developing and following efficient processes
  • Ability to organize and maintain accurate and timely records of contacts, activities, and schedules
  • Experience with Microsoft Project, Excel, and PowerPoint
  • Basic knowledge of SQL
  • Ability to travel regularly
  • Microsoft SharePoint work and site management
  • Microsoft Live Meeting
104

Research Coordinator Resume Examples & Samples

  • Experience in an academic medical center
  • Experience as a research study coordinator
  • Experience in cardiology clinical research
  • Familiarity with interpreting regulatory and contractual documents, identifying and resolving ambiguities, negotiating pricing and payment terms, and interpreting complex implications of research protocols
  • Knowledge of the Medicare Clinical Trials Policy and other federal, state and institutional clinical research regulations
  • Experience with using International Classification of Diseases, 9th Revision (ICD-9), Current Procedural Terminology (CPT), and Healthcare Common Procedure Coding System (HCPCS) billing codes in a clinical research environment
  • Strong working knowledge Microsoft Office Suite
105

Assistant Clinical Research Coordinator Resume Examples & Samples

  • Bachelor's degree in Psychology, Epidemiology, Public Health, Neuroscience, or Human Biology
  • Prior experience working with human subjects
  • Prior experience in behavioral sleep medicine
106

Research Coordinator Resume Examples & Samples

  • Prior experience in clinical or laboratory research in an oncology setting,
  • Knowledge of FDA and NIH requirements relating to research involving human subject
  • Experience in clinical trial development, implementation and analysis,
  • Experience with Microsoft Office, experience with case report forms (ideally paper and electronic)
  • Oncology clinical trial coordination experience
  • Knowledge of University of Washington/Fred Hutchinson Cancer Research Center/Seattle Cancer Care Alliance processes
107

Research Coordinator Resume Examples & Samples

  • Master’s degree in psychology, social work or counseling
  • Experience facilitating therapeutic interventions with groups
  • Experience working with high-risk mothers and children
108

Assistant Clinical Research Coordinator Resume Examples & Samples

  • Prior experience or exposure to conducting psychotherapy
  • Prior research experience including human subject interaction
  • Prior experience or exposure to behavioral sleep medicine
109

Assistant Clinical Research Coordinator Resume Examples & Samples

  • Demonstrated success with building partnerships with community agencies
  • Proficiency with Microsoft Office, ACT!, and REDcap
  • Skilled in effective risk management
  • Trained and skilled in motivational interviewing and stage-tailored interventions
  • Knowledgeable of nicotine addiction and its treatment
110

Assistant Clinical Research Coordinator Resume Examples & Samples

  • BA/BS in health sciences, physiology, biology; coursework or equivalent in behavioral health, gerontology, or related fields
  • Attention to detail and strong organizational and time management skills
  • Good interpersonal and communication skills are essential (both oral and written)
  • An excellent telephone manner and excellent verbal English communication skills
  • Experience with telephone and or in-person interviews in a research setting
  • Experience working with older adults and sensitivity to health issues and other issues of ageing
  • Experience with human subjects research, data collection and scientific procedures
  • Good computer skills, particularly with FileMaker, Excel and Word
111

Research Coordinator Resume Examples & Samples

  • A degree and/or prior work experience in chemistry or a related field
  • The ideal candidate will be a creative, enthusiastic self-starter who can react to the changing needs of the organization and take the initiative to bring to the attention of the PIs ideas, suggestions or solutions that better meet the goals of the unit
  • Excellent time-management and organizational skills and the ability to independently manage work priorities across multiple complex projects, meeting stringent timelines
  • Self-motivation and the ability to maintain a vision of overall program goals while managing and performing specific tasks with precision, accuracy, and meticulous attention to detail in an intense work environment
  • Strong collaborative skills for work with large, diverse groups, strong interpersonal skills, excellent written and oral communication
  • Experience with standard office software, reference management tools, email, financial modeling and budget preparation in Excel
  • Experience and aptitude with Mac- and Windows-based computing, and the ability to switch freely for cross-platform use
  • Experience with scientific manuscript preparation and editing
112

Research Coordinator Resume Examples & Samples

  • Assist in developing research plans and project designs; screening and scheduling research participants
  • Coordinating protocol activities and working with research participants in accordance with human subjects requirements
  • Administering questionnaires and testing procedures
  • Collecting, managing, and tabulating research data and ensuring its accuracy and security
  • Assist in preparing project reports and manuscripts; processing regulatory documentation for submission
  • Strong knowledge and understanding of the operational, logistic, and administrative requirements of research studies; ability to establish and maintain efficient work flow and administrative processes
  • Excellent organizational skills and attention to detail; skill in organizing resources and establishing priorities; ability to manage multiple tasks and complete them on time
  • Excellent interpersonal and communication skills; ability to interact with a diverse population of program participants
  • Demonstrated computer skills and proficiency with MS Office
  • Knowledge and experience with computer spreadsheets and database software
  • Strong written communication skills; ability to document project plans and activities, draft reports, and maintain project correspondence
113

Research Coordinator Resume Examples & Samples

  • Computer-based statistical software usage and the interpretation of findings in applied research settings
  • Conducts basic statistical analyses in database software, creates graphs and tables in spreadsheet software, and writes/edits in word processing software; prepares statistical and database reports, tables, graphs, narratives and questionnaires in print, electronic and web-enabled formats
  • Clearly and accurately communicate orally and in writing, complex and/or technical information
  • Proficiency in using computer databases, spreadsheets and word processing software
  • Excellent oral and written communication skills, critical thinking abilities and organizational skills
  • Knowledge of federal policy for the protection of human research subjects and other applicable regulations and standards
  • Proficiency in reviewing federal and private sponsors for grant opportunities and writing grant applications
114

Research Coordinator Resume Examples & Samples

  • Provide administrative support for meetings and training, as needed, including room set-up, materials, refreshments/meals and logistics
  • Assist with setting up departmental meetings
  • Coordinate travel requests (may include booking flights, hotel and ground accommodations)
  • Create, submit and manage expense reports
  • Provide data entry and project support to departments as assigned
  • Process various forms related to documenting activities of functional areas
  • Provide administrative support for clinical and technology grant programs
  • Tracks internal and external contracts, protocols, and legal agreements, such as with consultants, research partners, and ethics committees
  • Facilitates vendor relationships and assists with purchasing and order tracking
  • Process purchase orders, payments
  • Mailing of packages
  • Order and maintain office supplies
  • Assist in ad-hoc projects or other duties as needed. Additional assignments may be found in various functional areas
  • Minimum 5 years of experience supporting engineering teams or equivalent. Medical device or grant experience preferred. Experience within a research organization is a plus
  • Excellent communication (written, verbal), presentation and documentation skills
  • Comfortable with managing multiple projects simultaneously, with ability to switch focus between projects quickly
115

Research Coordinator Resume Examples & Samples

  • Maintains clear communication with customers regarding mutual expectations
  • May have physical requirement to lift no more that 10 lbs
  • May handle/work with biohazards
  • Training may be required for phlebotomy and EKG's/ECG's prior to performing on study participants
116

Research Coordinator Resume Examples & Samples

  • Data entry
  • Conduct data quality assurance checks
  • Clean research data Run queries / reports to fulfill data requests Interview research subjects
  • Perform literature searches and prepare literature reviews
  • Conduct patient interviews
117

Research Coordinator Resume Examples & Samples

  • Participate in data collection, management, and coordination and execution of study activities
  • Maintain excellence in research protocol adherence
  • Assist with regulatory compliance
  • Prepare and submit regulatory reports and reports to collaborators, and other parties as needed
  • Participate in study promotion, advertising, and outreach
  • Recruit study participants and manage their study participation
  • Assist with data analysis, writing results, and presentations for broad communication of study findings
  • Assist with writing, editing and reviewing of abstracts, reports and scientific articles for submission to conferences and publications
  • Develop PowerPoint or similar presentation tools appropriate to report research results to state and or national audiences
  • Sound analytical and organizational skills
  • Excellent interpersonal skills and ability to work collaboratively as part of a team
  • Ability to identify potential problems and trouble-shoot solutions
  • Proficiency in scientific/ research writing
  • Demonstrated application of specific research methods for clinical research, patient recruitment, and the management and conduct of research studies in diverse settings
  • Experience with research quality monitoring is preferred
  • Experience in communication (written and spoken) with medical providers, researchers, quality improvement teams, and patients is preferred
  • Experience with institutional review board (IRB) applications and renewals is preferred
  • Proficiency with REDCap database software is preferred
118

Clinical Research Coordinator, Senior Resume Examples & Samples

  • Ethical and participant safety considerations. Provide division or department-wide training in ethical conduct of research. Serve as expert resource to study teams as they design studies, so they include specific safeguards to ensure ethical conduct and protect vulnerable populations. Articulate the reasoning for an individual protocol's inclusion and exclusion criteria. Serve as a resource to help staff and patients recognize the difference between clinical care and clinical management of research participants. Independently develop documents related to safety and security. Serve as an expert resource for development and implementation of RDSPs, DSMPs, and Conflict of Interest plans across multiple studies or study teams
  • Data management and informatics. Use and train others in Electronic Data Capture (EDC) systems, technologies, and software necessary for study operations. Independently design CRFs to collect data according to protocol. Select methods of data capture and implement at the unit level. Investigate incomplete, inaccurate, or missing data/documents to ensure accuracy and completeness of data. Oversee the creation and use of queries, summaries, and reports. Develop system/framework for QA processes for multiple studies or for entire unit. Develop quality assurance systems for research data; ensure that QA SOPs are updated and followed by study teams. Implement quality assurance systems across multiple studies, or across entire unit, department or division. Recognize and report vulnerabilities related to security of physical and electronic data; recommend and lead implementation of processes, policies, and systems to ensure data security and data provenance
  • Scientific concepts and research design.Train others in the basic concepts of study design. Conduct and synthesize literature reviews, and independently develop proposals or protocols. Assess and determine solutions for operational shortcomings of proposals and protocols. Identify and collaborate with various stakeholders to ensure adequate design, implementation, and testing of study aims
  • Leadership and professionalism.Assist research colleagues in identifying efficiencies and improving process. May provide significant contribution and influence upon research work, activities, or productivity of project teams or across multiple groups. Network and encourage leadership opportunities for staff within a small work group. Lead a committee or task force. Actively seek out continuing education opportunities for self and study team members. Serve as a unit-wide expert resource for issues related to professional guidelines and code of ethics. Identify potential problems and risks to the participant, study, and institution. Maintain Duke and project specific training requirements. Develop solutions to proactively ensure unit,department, or division compliance with training requirements. Create strategies that enhance cultural diversity and cultural competency in the design and conduct of clinical research
  • Study and site management. Provide expert guidance to study team members to ensure participant care expenses have been set up correctly and that financial charges/expensed route in a timely manner; troubleshoot, escalate, and resolve issues. Collaborate with the financial analyst to establish financial monitoring systems. Coordinate with financial teams, PRMO, etc. Determine when financial reports are not working as planned and collaborate with sponsor and financial managers to troubleshoot. Develop study budgets. Coordinate operational plans for multiple research studies. Develop systems and documents including processflows, training manuals, and SOPs to be used unit, department, or division-wide. Work with sponsors/study teams to arrange required training. Lead site initiation, monitoring, and closeout visits and activities; provide feedback to the study team members. Develop and implement closeout procedures for multiple studies, unit, department, or division. Inform investigators and oversight organization regarding appropriate feasibility, recruitment, and retention strategies. Determine and implement alternative solutions to accomplish recruitment and retention milestones. Use system reports to ensure unit, division, or department compliance with institutional requirements and other policies; assist team members with understanding these requirements and policies. Oversee study teams# maintenance of Delegation of Authority Logs and training of KP on study specific duties
  • Communication and team science. Lead team meetings. Include others in decision-making, and escalate issues appropriately. Communicate with sponsors, subcontractors, or vendors and take action when communication has stalled. Act as an expert resource to junior staff liaising with sponsors, subcontractors, or vendors. Maintain training requirements. Develop solutions to proactively ensure study team members' compliance with training requirements. Evaluate the need for cultural diversity and cultural competency in the design and conduct of clinical research. Make recommendations to investigative team
119

Research Coordinator Resume Examples & Samples

  • Bilingual in Spanish
  • Phlebotomy trained
  • Current Baylor employees eligible to transfer are encouraged to apply
120

Research Coordinator Resume Examples & Samples

  • Work with subject matter experts to enable process for creating, improving, and expanding conventions for analyst workflows
  • Communicate directly with data analysts to improve and operationalize projects
  • Partner closely with Data Specialists and team members on protocol/process development for existing and future collections
  • Continuously evaluate data processing tools and processes and offer solutions to ensure they are efficient, high quality, and scalable
  • Experience with data processing, throughput analysis & reporting
121

Research Coordinator Resume Examples & Samples

  • Well developed research skills including experience developing questionnaires
  • Strong computer knowledge and experience with MS Office (Excel, Word, PowerPoint, Access), Outlook, and Photo Shop
  • Working knowledge of HTML coding and SPSS would be considered an asset
  • Demonstrated ability to review and identify trends and anomalies in data
  • Experience coordinating research projects independently
  • Ability to speak French is an asset
  • 1-2 years of market research experience, ideally in a retail environment
122

Assistant Clinical Research Coordinator Resume Examples & Samples

  • At least one year of relevant experience or an equivalent combination of experience, education, and training
  • Experience with maintenance of clinical study binders and with interface with electronic record-keeping methodologies
  • Familiarity with clinical registries/databases
123

Lead Clinical Research Coordinator Resume Examples & Samples

  • Ensures that protocol and subject milestones are entered and updated in timely manner in medical record and clinical trial management systems
  • Develops criteria for enrollment of prospective study subjects based on goals and objectives of project
  • Verify screening procedures are performed within protocol specific window
  • Assists in obtaining informed consent in accordance with applicable federal regulations and University policies
124

Research Coordinator Resume Examples & Samples

  • Proficient knowledge of SPSS (and/or R) and Microsoft Office Suite (especially Excel). Experience with E-Prime and FileMaker Pro, or the willingness to learn these applications
  • Experience with various stages of grant-funded research, including: preparation of grant applications, designing studies that fall within the scope of a project proposal, managing budgets, and reporting results to funding bodies
  • Careful attention to detail and an ability to anticipate future problems
  • Ability to create and maintain web pages and other multi-media projects
  • Data analysis skills
  • Comfort working with all age groups
125

Research Coordinator Resume Examples & Samples

  • Consult with research leadership to determine scope and extent of testing and analysis requirements
  • Determine equipment and materials needed to support testing and analysis efforts;, acquire materials as required
  • Oversee and coordinate set up and conducting of testing processes as previously determined
  • Analyze and document results of testing processes
  • Oversee or conduct calibration and maintenance of testing equipment; maintain required inventories of materials and supplies needed in testing process
  • Conduct ongoing review of testing methods and procedures; implement modifications to existing methods or develop new ones to improve process
  • May provide work direction and guidance to student assistants and other research support personnel
  • Education:High School Diploma, Technical Diploma, Associate's degree and/or two years of college level course work or an equivalent combination of education and experience
  • Work Experience:Six years of job related experience
  • Skills:Application of advanced laboratory testing processes and procedures specific to assigned specialty; analysis and documentation techniques, report writing, presentation and communications; work direction
  • Preferred Education:Bachelor's degree (BA/BS)
126

Research Coordinator Resume Examples & Samples

  • Previous experience in clinical trials required
  • Bachelor's degree or equivalent work experience in a healthcare related field required
  • Must be eligible and attain the status of Certified Clinical Research Professional (CCRP) or
  • Ability to work with and communicate to a diverse work force at all levels of the organization
  • Strong communication and leadership skills required
  • Must be able to adapt easily to change and lead others in a team environment
  • Strong computer and organizational skills
  • Understanding of ethical principles, culture and values of medical research, including Good
  • Minimum of three (3) years direct research experience as a Research Coordinator or similar
127

Research Coordinator Resume Examples & Samples

  • Master’s degree in Life Sciences or related
  • One year experience in research project management in the science or technology environment
  • In lieu of a degree, consideration will be given to an equivalent combination of related education and required work experience. 
  • Excellent written and oral communication skills with the ability to express ideas clearly and effectively
  • Familiarity with scientific and technical language
  • Strong organizational and time management skills; must have the ability to exercise sounds judgment in prioritizing tasks
  • Self-motivated and proven ability to work independently
  • Must be creative, thorough, and able to balance multiple tasks and handle confidential information with discretion
  • Ability to perform background research for specific grant programs, develop knowledge of federal and other granting programs, establish timelines and best practices for proposals, and function as an integral member of the proposal development team
  • Excellent interpersonal skills with the ability to represent PVM in a professional manner in interactions with internal and external stakeholders
128

Research Coordinator Resume Examples & Samples

  • Becomes familiar with all protocols assigned, as well as has a basic knowledge of all studies being conducted for Midwest Physician Administrative Services. For assigned studies, initiates study start-up activities including study initiation meeting, scheduling subject visits, along with scheduling any outside personnel or tests for these visits
  • Responsible for initiating and maintaining appropriate regulatory documentation and for facilitating all interaction between investigative site, sponsor and IRB
  • Evaluates volunteer subjects for potential study qualification in accordance with inclusion/exclusion criteria provided by study sponsor. Assists in subject recruitment
  • For qualified participants, initiates medical and social histories, physical exam, and physiological measures as indicated in protocol. Records this data in detail. Schedules study visits as required by protocols
  • Ensures appropriate laboratory, x-ray and other diagnostic examinations are scheduled and completed per study protocol. Oversees any outside services as required
  • Reviews medical, laboratory, and other diagnostic data on study patients. Notifies principal investigator of any abnormal values or any significant changes in these values. Notifies and follows up with subjects as required
  • Reports serious adverse events to principal investigator, sponsor and IRB (if required) in a timely manner. Follows up with subjects or subject's family members in accordance with procedures
  • Collects data requested by protocol. Ensures accuracy of data obtained. Collates and enters data into research charts, sponsor case report forms, and/or remote data entry equipment in a timely and precise manner
  • Ensures that all study drug/devices received is accurately documented and stored in locked location. Ensures that study drug/devices are maintained in appropriate temperature controlled environment. Verifies that all study drug/devices are correctly labeled, and packaged. Ensures that appropriate study drug/devices are dispensed to patient along with detailed instructions on use. Maintains accurate documentation of each of these along with return of test article
  • When studies require other supplies and/or equipment, coordinator will ensure their availability and ensure proper orientation has occurred prior to use
  • Ensures subject compliance with study treatment and study visits. Notifies sponsor of any deviations from protocol. Whenever possible, obtains permission prior to deviation, i.e., protocol exceptions
  • Schedules routine study reviews with sponsor monitors or appointed sponsor representative. Arranges access to all subject records for the indicated time period of review. Allows time to respond to monitor questions and to make correction to case report forms. Promptly responds to sponsor queries
  • Prepares for and completes close out procedures for terminated studies. Ensures all FDA, sponsor, and center regulations have been followed
  • Assist with training of other center personnel as directed
  • Works with other research coordinators and research assistants to provide back-up replacement during absences, and follow-up as needed
  • Provides health practices information and education to practice and study subjects regarding medications, diseases, diet, exercise, and any special procedures. Assists subjects by providing appropriate referrals to physicians, clinics, or agencies
  • May provide on-call service for study subjects during evenings and weekends on rotation basis with other research staff
  • Acts as a liaison for subject/physician telephone calls
  • Actively participates in clinical meetings, rounds, and departmental meetings
  • Participates in supervision and evaluation of research assistants
  • Participates in other center activities such as special projects, and any other duties as assigned by Director
  • Must take the certification test within 3 years of date of hire
  • Excellent clinical assessment skills
  • Detail-oriented and highly organized
  • Ability to understand technical research protocol
  • Able to make decisions independently and yet must be team oriented
  • Must possess ability to articulate and clearly communicate study information to patients, and other health care processionals
  • Professional demeanor with ability to interact with pharmaceutical/sponsor representatives, regulatory agents, medical center administration, medical staff, peers, and patients
  • At least one year of research experience as a clinical research coordinator is recommended
129

Research Coordinator Resume Examples & Samples

  • Conducting psychosocial intervention with parents across multiple time points
  • Organizing essential materials and measures to be given to families
  • Determining eligibility and recruiting research participants
  • Interfacing and communicating with medical providers
  • Collecting research data (both paper and electronic-based)
  • Scheduling follow-up visits with participants
130

Research Coordinator Resume Examples & Samples

  • Acquiring, managing, analyzing and archiving data
  • Geographic analysis
  • Meeting planning
  • Abstract, manuscript and grant editing
131

Research Coordinator Resume Examples & Samples

  • Recruit, screen, educate, and assist potential study enrollees and their families throughout the length of the study
  • Schedule research subjects’ appointments for tests and procedures
  • Responsibly handle and ship biospecimens
  • Retrieve and submit test results to appropriate party or data coordinating center
  • Enter study data from patients, families and medical records into a computerized database and/or on a case report form
  • Regulatory work including drafting, submitting, and amending new or ongoing research protocols for Institutional Review Board review
  • Ensure compliance with NIH and IRB regulations
  • Maintain records and regulatory documents
  • Work effectively with a team of research coordinator to ensure appropriate and high-quality cross-coverage of different protocols
  • Participate in weekly project meetings
  • Help meet study timelines as determined by the PI
  • Preferable to have experience using EPIC database for patient care records
132

Assistant Clinical Research Coordinator Resume Examples & Samples

  • Four year college degree in a related field
  • Experience working with healthcare professionals and clinical research participants
  • Experience with University related research policies and procedures
133

Research Coordinator Resume Examples & Samples

  • Requires skills in communicating, recruiting and data collection (qualitative and quantitative)
  • Knowledge in conducting heights, weights, GPS and CSA measurements, behavioral, and physical activity questionnaires
  • Skill and comfort with using PC computers including Word, Excel, Access, PowerPoint, and Survey Monkey (or equivalent) software programs
134

Trauma Research Coordinator Resume Examples & Samples

  • Develop and implement data collection processes related to specific research protocols
  • Responsible for managing database and performing data analysis
  • Assist with the preparation of Institutional Review Board (IRB) applications and reports for Annual Continuing Reviews
  • Plan and participate in research and performance improvement studies
  • Perform literature searches relevant to clinical research topics and references for bibliographies
  • Assist with the preparation of electronic presentation media for national meetings/conferences
  • Assist with the preparation of abstracts for national conferences
  • Compile, prepare, and review manuscripts for publication; consult with medical director regarding arrangements and compilation of content; proofread copyedited materials as required
  • Participate in clinical research initiatives
  • Coordinate and supervise activities with Clinical Research Organizations (CRO) that represent sponsored clinical trials
  • Works within defined protocols and current HIPPA regulations
135

Senior Clinical Research Coordinator Resume Examples & Samples

  • Responsible for data reporting and management, collection of source documents, use and development of case report forms, adverse events reporting, filing and archiving of study records, and resolution of data queries
  • Prepare and or complete regulatory related reports and IRB submissions. Maintain and organize study regulatory binders, enter all required study data on an ongoing basis
  • Ensure all study related samples are collected, properly prepared and shipped according to the protocol requirements and IATA/DOT regulations
  • Responsible for organizing and preparing for both internal and external auditing and study monitoring visits
  • May be responsible for tissue sample work
  • Provides day-to-day work direction to CRC I and II. Assists Clinical Research Managers with completion of performance reviews and provides input as needed for development and corrective action activities
  • Contributes to the development of research protocols and understands research design
  • Bachelor's Degree required and at least 3-5 years of equivalent experience required. Experience working in a medical or scientific research setting or comparable technology orientated business environment preferred. Performs primary duties with independence and has progressed to mentoring junior staff
  • Excellent organization and communications skills required. Strong interpersonal skills - ability to effectively interact with all levels of staff and externals contacts
  • Must be detail oriented and have the ability to follow-through. Ability to effectively manage time and prioritize workload
  • Must practice discretion and adhere to hospital confidentiality guidelines at all times
  • Must have computer skills including the use of Microsoft Office
  • Ability to coordinate PI initiated multi-center studies
136

Research Coordinator Resume Examples & Samples

  • Passion for customer empathy, people, and research
  • 2‐3 years’ experience in some form of recruiting, project coordination, or administrative support in a software or technology company
  • Ability to work in a fast‐paced, frequently changing environment while providing a superior level of support
  • Solid project management, organizational, and multi‐tasking skills. Must be proactive, take ownership, respond quickly, and have an unparalleled eye for detail
  • Proficient in Google Docs, Outlook and Excel
  • Experience managing relationships with multiple internal teams
  • Ability to solve problems creatively, proactively identify issues and inefficiencies, and provide resourceful solutions
  • Basic familiarity and interest in user research techniques a definite plus!
  • Effectively identify, recruit, and schedule participants for research studies
  • Handle all scheduling, coordination, and communication between the research team and research participants
  • Manage User Participation Agreements and track process
  • Create and manage screening surveys (Survey Monkey and Ethnio)
  • Manage participant incentives, including handling, purchasing, tracking, and accounting
  • Manage multiple participant databases
  • Conduct background research on participants and create participant profiles
  • Perform other tasks and support the team in projects aimed at maintaining and improving the research and participant recruiting program
  • Manage vendor relationships, such as third party research panel providers and rental facilities
137

Assistant Clinical Research Coordinator Resume Examples & Samples

  • Verbal and/or written fluency in Spanish or Mandarin is required
  • Strong interpersonal skills, sensitive to a range of participant needs
  • Previous experience with clinical research desired
  • Proficiency with REDCap and computer data entry
  • Excellent organizational skills and meticulous with record keeping
138

Research Coordinator Resume Examples & Samples

  • Gather and analyze data
  • Assist in the development of policies and procedures
  • Coordinate the development of research project reports
  • Review and analyze relative literature
  • Assist with modification of protocols
  • Consult with other units and community agencies concerning research project
  • Assign work; ensure proper workflow of the unit; act as lead worker
  • Serve on departmental and/or university committees as requested or required
  • May provide supervision to student employees and research assistants
  • Performs related duties based on departmental need
139

Research Coordinator Resume Examples & Samples

  • Demonstrated ability to complete detailed assignments in a timely and accurate manner
  • Demonstrated verbal, written, and interpersonal communications skills
  • Demonstrated customer service orientation that allows for effective interaction with study participants, patients, students, faculty and staff
  • Demonstrated ability to work with and adapt to new technology
  • Demonstrated ability to use MS Office at an advanced level, particularly Excel and its data analysis ToolPak, Word and PowerPoint
140

Research Coordinator Resume Examples & Samples

  • Coordinate participant recruitment, enrollment, and follow-up
  • Assist in development and implementation of recruitment strategies
  • Monitor data collection, cleaning and analysis
  • Act as liaison between subject coordinators and investigators
  • Coordinate meetings of project personnel
  • Responsible for incentive payment process
  • Responsible for processing IRBs and IRB compliance
  • A bachelor’s degree in a health related field is required; a master’s degree in Public Health is preferred
  • A minimum of three (3) year’s work experience in a clinical research related field is required
  • Candidate must have excellent communication skills, attention to detail, strong interpersonal skills, and organizational skills
  • Excellent computer skills, including expert knowledge of Microsoft Office products including Word, Excel, Outlook, Access and PowerPoint
  • Previous experience providing CTR/HIV counseling and testing
  • Candidate should have experience working with the LGBT community
  • Experience with online recruitment of research participants
141

Research Coordinator Resume Examples & Samples

  • Develops in-depth understanding of each study protocol to ensure all aspects of the protocol are adhered to in accordance with related Guidelines (such as FDA, GCP, and ICH)
  • Consults with PI regarding the appropriate administration of investigational product
  • Under the supervision of the Principal Investigator (PI), prepares and submits regulatory documents in an accurate and timely manner
  • In collaboration with the PI, incorporates clinical judgment and knowledge of protocol to identify potential study participants according to inclusion and exclusion criteria
  • Obtains informed consent according to GCP
  • Schedules subject visits and prepares labs/tests per protocol
  • Reviews and completes case report forms in timely manner
  • Conducts the investigational product according to the parameters of the study protocol and under the direction of the Physician
  • Conducts routine assessments to evaluate the subject’s response to investigational product, and communicates observations to related parties. Also, conducts ongoing assessments of the overall study execution within the facility/practice, communicating concerns to related parties
  • Educates, informs/updates the subject about the applicable study particulars and details
  • Documents subject information as it pertains to the clinical study according to the principals of ALCOA (Attributable, Legible, Contemporaneous, Original, and Accurate)
  • Meets with the study monitor to review, verify and correct all data entered onto the case report form and to ensure appropriate maintenance of study records
  • Reports consistently on the study, subject’s progress, complaints and issues to PI, study sponsor, or IRB as needed in a timely manner
  • Notifies PI, study sponsor and IRB of Serious Adverse Events according to protocol
  • Collects pre-study essential documents according to GCP and files appropriately in the study record
  • Maintains the study file and subject participant records according to GCP
  • Ensures appropriate storage, access, and maintenance of records pertaining to investigational product
  • Assist with various projects as assigned by direct supervisor
  • Additional responsibilities may include focus on one or more departments or locations. See applicable addendum for department or location specific functions
142

Equity Research Coordinator Resume Examples & Samples

  • Compile and present necessary industry information from Bloomberg, FactSet, and other industry sources
  • Create and maintain moderate-to-advanced excel documents, including but not limited to financial models
  • Assist with database needs, which may involve direct data entry, use of programs for uploading, organizing and manipulating the data in Excel
  • Assist with various analytical projects; prepare PowerPoint presentations for internal and external audiences and maintain related documents
  • Maintains calendar appointments, conference schedules and meetings for the research teams. Makes travel and accommodation arrangements, prepares itineraries and coordinates with teams to keep all parties informed of upcoming events, schedule changes, etc
  • Assists with the planning, coordinating and arrangements for various client and management meetings, luncheons, etc. Anticipates the needs for meeting rooms, menus, travel arrangements, presentation materials, etc
143

Research Coordinator Resume Examples & Samples

  • Functions as a team player with the department and works effectively with other coordinators in the department to foster an efficient and productive environment for Clinical Research
  • Implements and conducts multiple research projects in a timely and efficient manner
  • Prepares/Creates/OA's source documents prior to study start and according to SOP's
  • Collects data accurately and completes CRF's in a timely manner
  • Communicates to all appropriate research staff/supervisor/PI, and IRB of any deviations/violations from protocols as necessary
  • Communicates closely with Regulatory Coordinator to ensure the timely completion of these documents
  • Prepares on-site monitor visits, including pre-study, initiation and closeout visits
  • Maintains and updates essential documents as required by the FDA, IRB, Sponsor/CRO or any other regulatory agencies or funding agencies as necessary
  • Tracks patient visits in the study management software program as necessary
  • May assist Regulatory Coordinator in the preparation of protocol documents for IRB submission as necessary
  • Oversees and assists with data clarification forms as necessary and in a timely fashion
  • Aids in the development of research tools, such as spreadsheets or questionnaires
  • Develops, implements and continually evaluates patient recruitment strategies for effectiveness
  • Presents scientific statements or endorsements related to investigational devices/drugs with full disclosure
  • Provides information to research residents and staff regarding protocol requirements
  • Submits the IND to the FDA for investigator initiated studies and formulate/track regulatory documents necessary
  • Assists the staff physician and fellows, or independently writes, abstracts or manuscripts for submission to professional scientific meetings or journals
  • Performs study-related procedures and visits as required
  • Conducts follow-up visits of research subjects to evaluate progress and educate them regarding protocol, adverse events and compliance issues as requested
  • Reviews and documents lab and test results to ensure patient safety
144

Senior Research Coordinator Resume Examples & Samples

  • Associates Degree in business or related field preferred
  • 5+ years’ experience in related field is preferred
  • Familiarity with MS Office with a focus on Excel and PowerPoint
  • Exemplary attendance and job performance
145

Senior Research Coordinator Resume Examples & Samples

  • Provides technical and functional expertise in the area of Research studies. Recommends appropriate implementation plan. Monitors study routine to ensure progress of studies and reports to PI or Supervisor on progress. Oversees compliance with regulatory and granting agencies
  • Oversees coordination of a designated study or group of studies. In research projects, oversees recruitment of subjects, implementation of study procedures, and the collection and processing of data. Keeps accurate and up-to-date records
  • May be required to perform phlebotomy, electrocardiograms, or monitor vital signs on study participants. Educates family and contributes to the care and evaluation of subjects, including determining preliminary inclusion/ exclusion criteria. Reports findings to Supervisor or PI
  • Collaborates with physicians, investigators and other healthcare providers regarding subject care as necessary. Promotes respect for subjects' rights
  • Administers, scores and evaluates assessments as assigned and as related to study protocol. Collects data, confers with PI and forwards results to sponsor (internal or external)
  • Collaborates with PI and acts as a liaison between the Food and Drug Administration and drug companies on related issues. Adheres to and trains research staff on Good Clinical Practice, and regulatory and grant agency requirements. Follows protocol as developed. Keeps investigator informed of protocol changes or developments
  • Oversees availability of drug supplies and/or equipment for studies
  • Bachelor's Degree, in a field of Science, Behavioral Science or related field, required. Master Degree preferred
  • Minimum of five (5) years progressively responsible related experience
  • Demonstrates a high level of scientific knowledge
146

Research Coordinator Resume Examples & Samples

  • Submission and maintenance of regulatory documents and study records required by the Institutional Board (IRB), the Human Research Protection Office, sponsors and any other regulatory agencies
  • Participate in screening and recruitment of research study participants
  • Collect, process and ship specimens according to protocol requirements, in accordance with Haz-mat training and Good Clinical Practice requirements
  • Become proficient in use of IRB Manager, RedCap and other HIPAA compliant databases for data input and management
  • You may be required to participate in data collection and analysis
  • Participate in internal and external regulatory audits
  • Serve as liaison between PI, research team, study participants and personnel at collaborating institutions
  • Provide clerical and managerial support for research team as needed
  • Bachelor of Art or Science or related field
  • 2-3 years experience in human subject research coordination
  • Strong interpersonal, organizational and communication skills are required
  • Knowledge of medical and scientific terminology is preferred
  • Willingness to travel to multiple sites preferred
147

Research Coordinator Resume Examples & Samples

  • Bachelor’s degree or significant experience in research coordination
  • Minimum 3 years’ experience in a related area
  • Washington State Medical Assistant-Registered will be required with Swedish Medical Center facility application completed within 7 days of hire. Must obtain active license within 60 days of hire
  • Advanced knowledge of FDA research policies, other applicable federal regulations and/or GCP guidelines
  • Expertise in standard office software packages (Word, Excel, PowerPoint, etc.)
  • Familiar with and comfortable with research methodology and the “scientific method”: for conducting research projects
  • MA-R not required prior to hire
  • Certified Clinical Research Coordinator (CCRC) or similar professional research certification
148

Research Coordinator Resume Examples & Samples

  • Bachelor's Degree in Science, Healthcare, or related field. Significant experience in research coordination can be substituted for education
  • Minimum one year of experience in related field
  • Basic knowledge of FDA research policies
  • Must be well versed in scientific terminology
  • Familiar with research protocols and standard study requirements
  • Washington State Medical Assistant-Registered will be required with Swedish Medical Center facility application completed within 7 days of hire. Must obtain license within 60 days of hire
149

Research Coordinator Resume Examples & Samples

  • Primary anticipated responsibilities include: Data collection and management; Statistical analyses; Literature review; Contributing to computer simulation modeling efforts (developing and running computer models) The opportunity exists to participate in scientific manuscript preparation and writing. Support of manuscript preparation (e.g. communications with co-authors, Table/Figure development) is expected
  • A strong interest in medicine or medical research as a career
  • A strong interest in participating in clinical medical research
  • Proficiency with Microsoft Word and Excel, some familiarity with statistical and or database management software
  • Willingness to learn and work with computer-based simulation models
  • An ability to perform medical literature searches
  • Strong database management skills, for data extraction from national or local patient databases
  • Excellent communication skills, including ability to interact with physicians, patients and researchers
  • Strong work ethic, excellent organization skills, and meticulous attention to detail
150

Bft Research Coordinator Needed for Mgh Surgery Resume Examples & Samples

  • Serves as office liaison between Institutional Review Board (IRB) and Lab safety, processing requests for new research protocols, completing continuing reviews for ongoing studies and submitting amendments for any changes to a study
  • Prepares service contracts and standing purchase orders as well as material transfer requests
  • Prepares and organizes materials for internal and external dissemination
  • Schedules meetings, updates calendars and makes travel arrangements
  • Answers telephones; places/returns telephone calls as requested
  • Retrieves, screens and triages office mail
  • Performs photocopying, faxing, filing as requested
  • Orders office supplies, forms, stamps, etc. as needed and maintains spreadsheet of all orders
  • Performs check requests, coordinates travel arrangements and prepares reimbursement materials
  • Arranges for outside visitors, medical students, etc. as requested
  • Participates in weekly CORE staff meetings by preparing agenda and facilitating meeting
  • Performs/participates in special projects as may arise from time-to-time
  • Ordering and picking up food supplies for laboratory
  • Completing onboarding and HR paperwork for incoming interns and trainees
  • Maintenance of lab website
  • Associates degree required with Bachelor’s degree helpful. Microbiology and/or Molecular Biology skills a plus
  • Ability to multitask and work accurately
  • Neat and orderly work habits
  • Management of IRB documentation
  • Coordinating events/meetings
  • Exceptional computer skills (including MS Word, Outlook, Internet, and Spreadsheets)
  • Is knowledgeable and compliant in all hospital, State and Federal regulatory requirements including HIPAA, Joint Commission
151

Melanoma Translational Research Coordinator Resume Examples & Samples

  • Incumbent will supervise post-doctoral fellows and research technicians in the Flaherty lab
  • B.A/B.S. required
  • Minimum of 3-4 years related experience required
  • Proven success and experience facilitating multi-disciplinary interaction
  • Ability to work independently with general direction, moderate oversight and day-to-day instruction
  • Ability to handle multiple complex projects simultaneously
  • Commitment to excellence
  • Demonstrated ability to take initiative based on sound judgment
  • Knowledge of MGH/Partners/HMS conflict of interest rules
  • Flexibility and willingness to take on broad range of tasks
  • Demonstrated ability to work effectively with colleagues at all levels, from administrative assistants to academic, hospital, and corporate collaborators
152

Research Coordinator Resume Examples & Samples

  • Assist in data collection, quality review of data, data analysis and data presentation and publication
  • Coordinate and administer questionnaires, and assist with procedures for obtaining patient screening and recruitment as needed
  • Coordinate and perform duties for approved research projects according to defined protocols and procedures
  • Coordinate recruitment efforts, training, and supervise research staff as needed
  • Follow appropriate research policies and procedures including all applicable laws and regulations and maintains scientific integrity including accurate data storage
  • Follow the mandatory reporting procedures for any incident or serious event that did affect or potentially could have affected the clinical care of any patient/participant
  • Revise, renew and maintain IRB approval, protocols and consent forms for studies
  • Masters degree in psychology, health administration, or other related field is required
  • Five years of relevant research and/or administrative experience in a clinical or academic setting is required
  • Prior supervisory experience strongly preferred
  • Computer Skills (Microsoft Office Products)
  • Excellent communication skills both verbal and written
153

Research Coordinator Resume Examples & Samples

  • Provide administrative assistance and support to TM Labs Leadership as needed
  • Draft, prepare, and send meeting invitations on behalf of TM Labs Leadership
  • Assist in the editing of presentations and reports to ensure high-quality deliverables
  • Maintain/Update the TM Labs Portal (SharePoint)
  • Assist with internal and external outreach as needed to support TM Labs projects
  • Work with the Chief of Staff to ensure TM Labs deadlines and commitments are met
  • Compile monthly progress reports on TM Labs projects
  • Support Research Scientists and Consultants on various project needs
  • Organize materials into online repositories
  • Create supporting documents for research processes and activities
  • Develop data dictionaries and keeping records for key data sets
  • Coordinate interactions between TM Labs staff and internal stakeholders
  • Effective time management skills and ability to work well under pressure
  • Excellent organization, multitasking, and prioritization skills
  • Excellent written and oral communication skills; equally comfortable working via email and phone
  • Ability to work across teams and build relationships with staff at all levels
  • Demonstrated experience using Microsoft Office, specifically Outlook, Excel, and PowerPoint
  • Superior problem solving ability; ability to learn substance of research quickly
  • Demonstrated initiative, persistence, and resourcefulness
154

Research Coordinator Resume Examples & Samples

  • Bachelor's degree (preferably in science, healthcare, or other related field). Significant experience in research coordination may be substituted for educational requirements
  • Minimum of three years experience in related area
  • Expertise in standard office software packages (Word, Excel, PowerPoint, etc.), standard office equipment (photocopiers, facsimiles, telephones, pagers, etc.)
155

Research Coordinator Resume Examples & Samples

  • 1) BA/BS in psychology, biology, engineering, or related field
  • 2) two years of research experience
  • 3) demonstrated organizational skills or experience with data management
  • 4) desire to succeed in a fast-paced research environment with multiple duties
  • 5) Demonstrated attention to detail, organizational skills, and excellent written and oral communication skills
  • 6) Proficiency with Word, Excel, and PowerPoint or equivalent
  • 1) Proficiency with MATLAB, statistical analysis, and/or experience with web development
  • 2) Experience with writing and following IRB protocols
156

Research Coordinator Resume Examples & Samples

  • Organizes study related activities to ensure compliance with FDA, GCP, IRB, HIPAA, SOPs, sponsor and institutional regulations and requirements.Serves as contact for subjects, study personnel, the department, the school, pharmacy and other ancillary service departments, Institutional Review Board (IRB) and study sponsor
  • Pre-screens patient records and assesses patient eligibility. Coordinates study participant activities including screening, recruitment, orientation, correspondence, and ongoing patient education about clinical trials. Schedules and confirms subject appointments, tests and procedures with internal and external providers as needed. Coordinates with labs, pharmacies, hospitals and other ancillary units for protocol required tests/procedures/drug administration/reimbursements for upcoming patient visits
  • Collects patient data, inputs and analyzes for research studies. Maintains accurate, complete and timely records, including source documents, consent forms, case report forms, protocol documents, and regulatory documents, as required by sponsor and institutional guidelines
  • Coordinates with labs for sample and data collection, sample processing and shipment for each study. Orders supplies and equipment. Researches and develops recommendations for new supplies/equipment purchases
  • Tracks, reports, documents and enters data internally and in sponsor’s system for patient visits and study status.Provides updates to and resolves queries with ancillary departments including the accounting department
  • Submits protocols to IRB, completes study continuing review, amendments, and reportable events to IRB in a timely and accurate manner, and closeout the study with IRB
  • Schedules, prepares and participates in initiation and closeout visits, monitoring visit and external/internal audits. Provides timely response to queries from sponsor and/or auditors, and close the study with sponsor
  • Participates in research meetings with PIs to present research updates and gather future research plans. Regularly meets with the department to provide research/workload updates and discuss potential issues and plans
  • Documents and improves standard operating procedures, researches and prepares guideline documents and reports as assigned
  • Assists in organization and preparation of grant proposals. Gathers documentation such as annual reports and detailed budgets for inclusion in proposal. Assists investigators in developing research proposals and budgets. Interfaces with funding and regulatory agencies to exchange information
157

UX Research Coordinator Resume Examples & Samples

  • 1-2 years experience in coordinating tasks that support research activities, including: participant recruitment, scheduling, and communication
  • Detail-oriented, organized, resourceful, and able to work independently
  • Strong interpersonal, communication, and collaboration skills
  • Proficiency with Google office productivity tools, including email, calendar, spreadsheets, word documents, and presentations
  • Interest in user experience research and design
158

Research Coordinator Resume Examples & Samples

  • Master's level or higher degree, or equivalent combination of experience and education in public health, gerontology, or related field
  • Demonstrated experience in writing/editing and submitting manuscripts for publications and scientific journals
  • Demonstrated ability in writing grants and research proposals
  • Knowledge of the contract and grant proposal submission process to federal, state or private funding organizations, including the online submission process
  • Demonstrated experience in coordinating a research project
  • Knowledge of human subjects and Institutional Review Board and other federal research policies and procedures
  • Attention to details and ability to analytically assess and compile written responses
  • Experience in multi-tasking and ability to perform under stress and deadlines
  • Knowledge of UCSD policies and procedures
159

Technical Research Coordinator Resume Examples & Samples

  • Limited position, may become career**
  • Demonstrated knowledge and skill in current and emerging Internet and social media platforms
  • Some expertise in computer science and engineering
  • Social and team-oriented
  • Extremely organized and detail-oriented
  • Online/social media marketing and Technology knowledge
  • Experience either as a journalist or as an author/co-author on previously submitted/published research-related manuscripts
  • Master's Degree and at least 2 years of project management experience
160

Research Coordinator Resume Examples & Samples

  • Ability to confidently and independently write research manuscripts and briefs that will convey our research to local clinics and organizations
  • At least 2 years of research experience carrying out behavioral interventions
  • Demonstrated knowledge and skill in the use of social media platforms
  • Demonstrated statistical analysis skills in order to analyze research results to determine study outcomes
  • Ability to establish and maintain cooperative working relationships
  • Willingness to work occasional evenings and weekends
  • Organizational skills to maintain records and coordinate other tasks as required
  • Ability to communicate with others about sensitive behavioral issues, including drug use and criminal behavior, and frequency of high-risk behaviors
  • Skill in speaking and writing to persons of various social, cultural, economic, and educational backgrounds
  • Demonstrated knowledge of personal computers and relevant software programs (e.g., data entry, word processing, spreadsheets)
  • Willingness and ability to maintain confidentiality of subjects
  • Ability to communicate clearly and effectively, verbally, and in writing, with subjects, staff, and supervisors
  • Skilled in keeping accurate and timely records
  • Ability to work independently and report to Principal Investigator on a regular basis and in a timely manner
  • Ability to manage competing demands/assignments/deadlines
  • Ability to be punctual and maintain a satisfactory attendance record
  • College or graduate degree strongly preferred
  • Bilingual English/Spanish
  • Experience in data entry and cleaning
  • Experience working with substance abusers and/or with HIV-positive populations
161

Background Check Research Coordinator Resume Examples & Samples

  • Make sound employment adjudication decisions to mitigate legal risk
  • Adhere to all department guidelines and procedures
  • Regular, dependable attendance & punctuality
  • High school diploma or general education degree (GED) required
  • Prior experience in conducting applicant interviews and/or pre-employment screening preferred, but not required
  • Ability to collaborate with outside vendors and internal clients at all levels
  • Basic math functions such as addition, subtraction, multiplication and division
  • Must be able to work independently with minimal supervision
  • Retail business acumen; understanding how retail organizations operate and how roles work together
  • Must possess the ability to prioritize a changing workload, with a high sense of urgency
162

Assistant Clinical Research Coordinator Resume Examples & Samples

  • BA/BS in Psychology, or related field of study
  • Research experience, preferably with eating disorders
  • Good understanding of psychopathology and DSM V diagnoses
  • Comfort with working with children and their families
163

Research Coordinator Resume Examples & Samples

  • Administer questionnaires, and assist with procedures for obtaining patient screening and recruitment as well as obtaining research specimens
  • Assist in data collection and data entry and quality control of data
  • Assist in hypothesis generation, data collection, data analysis and data presentation and publication
  • Complete online IRB certification modules 1 and 2 (Research Practice Fundamentals) in accordance with Health Sciences at the University of Pittsburgh
  • Follow the mandatory reporting procedures for any incident or serious event that did affect or potentially could have affected the clinical care of any patient
  • Perform duties for approved research projects according to defined protocols and procedures including appropriate collection, recording, and storage of data
  • Process, label, store and ship blood specimens obtained from research subjects
  • B.A. degree, or equivalent combination of experience and training - including 3-5 years of experience in coordinating multiple aspects of research projects (patient recruitment, assessment, treatment planning, and data collection,) required
  • Previous multi-center Clinical Trial experience is strongly preferred
  • Working knowledge of Research regulations and IRB protocols is strongly preferred
  • Ability to accurately collect, and store research data
  • Demonstrated ability to effectively communicate with patients, staff and investigators as well as maintain patient confidentiality
  • Ability to work independently, must be able to work a flexible schedule based on study needs
  • Ability to interact with patients/study participants and research and medical staff
  • Knowledge and skills necessary to provide care and/or interact appropriately to the ages of the patients served by his/her assigned unit as specified below
  • Knowledge of the principles of growth and cognition over the life span and possess the ability to assess data reflective of the patients status and interpret the appropriate information needed to identify each patients requirements relative to his/her age-specific needs and to provide the care needs as described in the departments policy and procedures
164

Research Coordinator Resume Examples & Samples

  • Should have prior experience with coding behavior observation using a qualitative analysis software
  • Interest and enthusiasm for topics related to child development and health
  • Ability to work several hours coding observation data
165

Research Coordinator Resume Examples & Samples

  • Ability to work both independently and collaboratively
  • Knowledge and application of scientific procedures and research techniques
  • Ability to mentor others
166

Research Coordinator Resume Examples & Samples

  • Schedules subjects for protocol-related evaluations. Collaborates with physicians, investigators and other healthcare providers. Promotes respect for subjects’ rights
  • Bachelor’s Degree, required
  • Redcap preferred
  • Prior Clinical Trial or Sponsor Trial experience, preferred
  • Ability to take initiative and work interdependently, meet deadlines with a sense of urgency, multitask, adjust to shifting priorities and work under defined rules and regulations
167

Research Coordinator Lead-swedish Cancer Institute Resume Examples & Samples

  • Bachelor's degree required, preferably in science, healthcare, or other related field. Significant experience in a supervisory capacity may be substituted for educational requirements
  • Washington State Medical Assistant-Registered will be required with Swedish Medical Center facility application completed within 7 days of hire. Must obtain active license within 60 days of hire. Employee will not be authorized to practice independently until registration is obtained
  • Minimum of seven years experience in related area
  • Certified Clinical Research Coordinators (CCRC) or similar professional research certification preferred
168

Lead Clinical Research Coordinator Resume Examples & Samples

  • Serves as liaison between clinical research team and hospital/research institute senior leaders. Provides strategic direction on clinical research portfolio and clinical research pipeline, issue resolution and quality improvement initiatives
  • Interfaces between clinical staff, the Office of Sponsored Research, Research Administration, PIs, clinical research staff, and external entities to create and adhere to programmatic budgets and strategic plans
  • Interfaces with clinical staff to identify patients eligible for clinical trials across one or multiple sites of service
  • Interfaces with patients and their families to provide education regarding investigational studies, and requirements of participation to assure they are informed prior to obtaining written consent. Completes required follow-up and active patient monitoring per study protocol at one or multiple sites of service
  • Plans, coordinates, and manages all activities pertinent to the specific clinical trials, ensuring patient safety, good clinical practices, and compliance with the protocol and regulatory agencies
  • Bachelor's degree or RN/BSN; Master's degree preferred in related field
  • Generally has at least 6 years of related experience
  • Current research-related certification from accredited program (e.g. CIRA, CCRP) required or ability to obtain within 6 months of hire
  • Role models clinical research operations and interfacing with PI/clinical research team; has proven track record of fostering relationships with external constituents; demonstrates in- and out-patient clinical issue resolution; has worked to develop a research presence nationally (e.g. publications and presentations)
  • Follows standard and/or other appropriate precautions using personal protective equipment as required
169

Senior Clinical Research Coordinator Resume Examples & Samples

  • Interfaces between clinical staff, the Office of Sponsored Research, Research Administration, PIs, clinical research staff, and external entities to identify clinical research pipeline and completes protocol budgeting, feasibility, and initiation
  • Provides in-service education to the appropriate hospital personnel in the departments involved with the investigational study
  • Interfaces with patients and their families to provide education regarding investigational studies, and requirements of participation to assure they are informed prior to obtaining written consent
  • Completes required follow-up and active patient monitoring per study protocol at one or multiple sites of service
  • Bachelor's degree or RN/BSN
  • Generally has at least 4 years of related experience
  • Current research-related certification from accredited program (e.g. CIRA, CCRP) required or ability to obtain within six months of hire
  • Driver's license may be required depending on facility requirements
  • Has mastered the components of clinical research operations, works with PIs/clinical research team and clinical teams to resolve issues, initiates new clinical research trials, sets study budgets, and serves as a point person for external constituents
170

Market Research Coordinator Resume Examples & Samples

  • Maintain the Group Rooms Control Log (GRC) and FDC database
  • Daily logging and distribution of all incoming leads, Generate the Weekly and End of Month Sales Reports
  • Prepare and distribute monthly production forecast, Enter pick-up on a daily or weekly basis
  • Must have full knowledge of the Sales Administration Manual and ensure that procedures are being followed
  • Responsible to maintain monthly recap with reservations to insure GRC blocks are the same as Reservation blocks
  • Assist in 90 day forecasting process, Attend Weekly Support Staff Meetings
  • Types and distributes all correspondence, including letters, emails, proposals, contracts, etc. for assigned managers
  • Ensures that all correspondence is 100% accurate
  • Maintains account files and ensures that all information is included in file, i.e. post-convention reports, letters, fax information
  • Professionally answers calls to the sales office and accurately takes messages, as applicable
  • Enters group information (sites, resumes) in computer database
  • Assists in generating proposals with information accurate and specific to each client
  • Creates and updates documents and spreadsheets for DOSM, as needed
  • Takes detailed inquiry leads and submits to appropriate manager
  • Inputs amenities into compute for VIP clients and processes paperwork (amenity card, receipt signature from Room Service.)
  • Orders office supplies and maintains function of office equipment
  • Good verbal/written communication skills
  • Maintain a professional business appearance, attitude, and performance
  • Ability to effectively use Microsoft Word, Publisher, Outlook, and Excel is required
  • Must have good organizational skills, attention to detail and be able to multitask
  • Previous hospitality or administrative experience is required
  • Experience in a sales environment is strongly preferred
171

Research Coordinator Resume Examples & Samples

  • Experience as a research professional for investigator-initiated research projects, with expertise in grant and protocol management including oversight of daily research operations
  • Excellent written and verbal communication, including patient interactions, consulting, and customer service skills
  • Proficiency with standard MS Office software, including Word, Excel, Access, and Power Point
  • Strong internal and external customer service skills
  • Ability to adapt and respond appropriately to competing priorities in a fast-paced environment
  • Self-motivated, self-starter who takes initiative to improve existing processes
172

Senior Clinical Research Coordinator Resume Examples & Samples

  • With direction from the PI, oversees study operations for all NeuroNEXT studies
  • Establishes and monitors timelines and benchmarks for study implementation, recruitment, and completion
  • Coordinates and supervises efforts for all NeuroNEXT studies and provides guidance to the study specific staff on required network training, protocol compliance, meeting recruitment goals, performing study procedures and managing data collection
  • Monitors study performance for subject enrollment goals and data acquisition in accordance with the protocols and conveys information to NeuroNEXT PI
  • Serves as primary resource for all regulatory and operational aspects of the NeuroNEXT site, overseeing submission and maintenance of documentation to the CIRB
  • Interacts directly with involved staff at the UM sub-sites (MCH and JHS), study sponsors and monitors, the NINDS, other network sites, the Clinical Coordination Center, and the Data Coordination Center
  • Designs and implements quality assurance systems to assure protocol compliance
  • Ensures compliance with applicable NeuroNEXT, FDA, NIH and other regulatory agencies' requirements
  • Develops and maintains Standard Operating Procedures for the UM site
  • Oversees collection and integrity of trial data at the site
  • Serves as the primary site liaison and appropriately triages correspondence to relevant parties
  • Meets regularly with investigators and coordinators involved with NeuroNEXT trials
  • Supports local research infrastructure by organizing monthly Neurology Clinical Research Roundtable sessions, raising awareness about the network, and engaging faculty in network initiatives
  • Assists with budget monitoring of NeuroNEXT study funds
173

Market Research Coordinator Resume Examples & Samples

  • Assist with the development of sales presentations and marketing strategies
  • Administrative support including phone coverage, internal brand/hotel and client communication, travel coordination, expense reports and tracking, marketing calls and meeting preparation (prepare weekly minutes from internal meetings) and follow-up as well as other administrative tasks
  • Maintain and update revenue production from marketing campaigns
  • Assist with the development of internal and external presentation materials including PowerPoint presentations, webinar content, advertisements, marketing and collateral
  • Maintain balance sheets, expense checkbooks and invoices
  • Assist with other projects as needed
  • Strong attention to detail, well-organized and ability to deal efficiently under pressure and multi-task while being personable
  • Highly skilled with Microsoft Excel, including the ability to use filters and pivot tables
  • Proficient with MS Word, MS PowerPoint and MS Outlook
  • 2-4 years of administration experience preferred but not required
  • College degree or equivalent required
174

Research Coordinator Resume Examples & Samples

  • Preparation and design of research and study projects
  • Capacity building for research and study team
  • Research and Study implementation
  • Data Management and analysis of study and research results
  • Experience in design and implementation training/Capacity-building strategies on nutrition interventions, especially maternal and child nutrition
  • Effective in written and oral communication; be able to speak and write with a standard of English
  • Computer literate in MS Word, MS Excel, MS PowerPoint, e-mail and internet
  • Familiarity with the Ministry of Health policies and programs aimed at improving nutritional status of women and children
  • If you cannot see the job announcement on World Vision website through the link above(1): Please copy job ID: NO-FY17-F017 to be your email subject ONLY and attach your completed Application Form, CV and Cover Letter to Email: cam_recruitment@wvi.org or contact us at Tel: 023 216 052 Ext: 121
175

Research Coordinator Resume Examples & Samples

  • Conceive, author and edit grant proposals, exhibiting strong expository as well as persuasive prose. Possess a high-level command of grammar and spelling
  • Conceive, plan and conduct research for trauma grant opportunities and funding using advanced search techniques. Possess proficiency in searching funding sources through on-line databases and printed resource material. Filter grant-making prospects and project feasibility of funding
  • Assist the members of the Division of Trauma Surgery and Surgical Critical Care in the development of documents and proposals in response to Requests for Proposals from private foundations and governmental funding sources. Includes preparation of the RFP
  • Customize grant proposals in accordance with each grant-making organization’s preferences and follow exactly each grant-making organization’s guidelines
  • Prepare project reports, financial and statistical reports, surveys, documentation and analyses as required by grant-making organizations to ensure compliance with all requirements
  • Communicate and report regularly with the Chief, Division of Trauma Surgery & Surgical Critical Care, Director of Trauma Center & Trauma Program, on the status of these activities
  • Facilitate and enforce adherence to research deadlines
  • Exhibit superior communication and information gathering skills to work as a team playerin the smooth operation of an active and highly visible academic program
  • Develop and compose various non-routine communication pieces to include: solicitation letters, case statements and funding proposals
  • Acquire and maintain sound knowledge and understanding of the CHI Health Creighton University Medical Center and the projects, programs, services, equipment, technology and/or capital needs for which funding is sought
  • Manage information ethically, accurately and confidentially
  • Maintain a professional attitude with patients, visitors and other hospital personnel while assuring confidentiality of patient information and other hospital information
  • Complete grant, journal, and publication writing duties and responsibilities as assigned. Maintain standards of publication and authorship
  • Work effectively and collaboratively in a diverse and multi-cultural environment
  • Maintain academic and clinical professionalism, including interactions with collaborating academic centers and departments and with patients/families
  • Build and maintain databases as required by grantees and work product
  • Reports regularly to the Chief, Division of Trauma Surgery & Surgical Critical Care, Director of Trauma Center & Trauma Program
  • Two - five years’ experience in clinical research
  • Two – five years’ experience in administering grant projects
  • Ability to work independently without supervision
  • Demonstrated advanced computer skills/expertise using Microsoft Word, - Excel, PowerPoint, Access and grant management software
  • Strong knowledge of clinical grant management
  • Excellent oral and written communication skills, excellent knowledge of grammar and sentence structure
  • Excellent listening, problem solving and planning skills
  • Enthusiasm for, and understanding of, building external relations
  • Strong leadership and motivational skills
  • Strong skills in human relations and diplomacy
  • Ability to work efficiently and independently on multiple simultaneous projects
  • Ability to think critically and creatively
  • Bilingual or multilingual skills preferable (not required)
176

Research Coordinator Resume Examples & Samples

  • The first is ensuring placement of clinical trials within targeted and appropriate dialysis units or CKD practices
  • The second is organizing resources including PIs
  • The third is overseeing the execution of the studies, ensuring successful completion within GCP, with minimal participant attrition
  • The fourth is mentoring and involving the right TMs in the village to assist in study execution
  • The fifth is participating in the cultivation and nurturing of physician relationships
  • Individuals who take on the role of Regional Study Coordinator generally have some defining qualities. These qualities include the ability to manage complex and strategic projects with a focus on core task accomplishments. This individual will have a drive to continuously educate themselves and understand both clinical and regulatory components of clinical trial execution. They will also possess the ability to communicate well, be tenacious, flexible, and versatile
  • Provides overall management and execution of studies as assigned
  • Ensures DVA sites are committed to the project
  • Leads study team
  • Acts as a liaison between the physicians, sponsors and TMs
  • A deliverable revenue/ebitda goal for each budget year
  • Mentor and build the capacity of village TMs to assist in the conduct of clinical trials
  • Performance-based rewards based on stellar individual and team contributions
177

Research Coordinator Resume Examples & Samples

  • Must have excellent organizational and interpersonal skills
  • Must possess excellent written and verbal communication skills
  • Must have ability to multi-task and work independently
  • Proficiency using software programs such as Microsoft Office (i.e. Word, Excel, PowerPoint, and Outlook)
178

Research Coordinator Resume Examples & Samples

  • Oversee the work of healthcare analysts, biostatisticians, and Medicaid policy experts in synthesizing results from qualitative and quantitative data
  • Lead deliverable production to ensure that internal and external reports and/or deliverables adhere to project specifications, are submitted on time, and meet or exceed quality standards. Develop quarterly progress reports for the sponsor
  • Write reports and develop complex charts, tables, and presentations from synthesized information that is provided by bio-statisticians and senior faculty in the team. Assist with interpretation of results and development of program/policy recommendations
  • Oversee data requests and data collection from partner state agencies and supervise administrative staff assisting with project coordination
  • Develop and maintain a comprehensive project plan to guide the day-to-day tasks, operations, and communications. Build and manage relationships with vendors for qualitative data collection
  • Master's Degree in social/behavioral sciences, public health, or related field and five or more years of professional experience
  • Previous experience in health policy research and/or evaluation of healthcare programs is strongly preferred
  • Experience with research project management is a plus
  • Demonstrated experience with writing of complex reports
  • Ability to work independently and ability to collaborate with external constituencies
  • All applicants should have clear ability to take initiative and manage time
179

Research Coordinator Resume Examples & Samples

  • Theoretical knowledge of biomedical informatics, computer science or related field as typically acquired by a Bachelor's degree, or an equivalent combination of education and experience
  • Demonstrated experience organizing large volumes of data using creative tools, logs and databases created to use with multiple research projects
  • Demonstrated experience interpreting/coordinating research protocols and the corresponding data requirements. Demonstrated experience with human subjects research and processes
  • Demonstrated knowledge of library referencing procedures, knowledge of PubMed searches and Reference Manager. Demonstrated experience conducting literature reviews and internet searches for project-related clinical studies
  • Demonstrated experience with grant proposal preparation, agency rules and regulations, particularly NIH
  • Experience with website content management
  • Demonstrated experience with multiple computer programs such as Microsoft Office (Excel, Word, Outlook, Power Point, and Project), Adobe (Photoshop, Acrobat, and Illustrator), EndNote or equivalent, SharePoint, Joomla or equivalent, and Camtasia or equivalent
  • Strong decision making skills and ability to use independent judgment and discretion to quickly set priorities and establish new procedures when needed. Demonstrated ability to research, analyze, recommend, communicate, and implement solutions. Must function independently with minimal direction
  • Experience with event planning, outreach, and social media marketing
180

Research Coordinator Resume Examples & Samples

  • Creation of site-specific SOPs
  • Monitor on-line recruitment
  • Manage and schedule follow-up as specified per protocol
  • Complete, organize and maintain all study documentation as directed by the supervisor
181

Donor Database & Research Coordinator Resume Examples & Samples

  • Ensure prompt and accurate processing and documentation of donor gifts, integrating with Financial Edge software, complying with IRS regulations and department procedures
  • Develop and produce queries, donor profiles, dashboards, custom reports, and mailing lists to support department goals. Manage any data mergers
  • Make recommendations on data organization and integrity; develop best practices; train staff in best practices and enforce procedures
  • Create and process prompt donor acknowledgement letters to include: thank-you’s, honor/memorial gifts, new and lapsed donor reports, pledge and past-due reminders
  • Use Kintera Sphere software to create and update online donation portals and registration webpages
  • Work closely with finance department to reconcile all gifts and records
  • Conduct prospect research in coordination with development team. Research and master tools to facilitate this process. Manage research and prospect modules in Raiser's Edge
  • Assist in event planning using data management skills, which may include: invitation and mailing lists, registration and financial tracking, and specific guest correspondence
  • Coordinate all software upgrades with HCMC IT department
  • Serve as the key contact and administrator to Blackbaud to maintain Raiser's Edge and all relevant modules. This includes maintenance, upgrades and system changes
  • May provide work direction for future data entry staff
  • Bachelor degree in a related field or an approved equivalent of education and experience
  • Experience with prospect research tools, mailing list acquisition and management, fundraising analysis and reports
  • Systems expert and ensures accountability to structured processes
  • Ability to manage workload independently and build a network of resources
  • Knowledgeable of best practices within donor relations
  • Strong communication and diplomacy skills
  • Assertive and able to push back when appropriate
  • Collaborative and effective team player across diverse groups
  • 2 years experience in donor database management and Raiser's Edge highly preferred
  • Experience with safety net hospitals preferred
182

Practice Research Coordinator Resume Examples & Samples

  • Ensures availability of drug supplies and/or equipment for studies. Maintains drug accountability logs
  • Bachelor’s Degree, in a field of Science, Behavioral Science or related field, required
  • Certified in Haz-Mat Training for packing and shipping, as needed per study protocols, required
  • Certification required for performance of venipuncture, electrocardiogram and vital signs, as needed per study protocols
183

Research Coordinator Resume Examples & Samples

  • Knowledge of Microsoft Office (i.e. Word, Excel, Outlook, PowerPoint) and Atlas.ti
  • Skill in completing assignments accurately and with attention to detail
  • Strong interpersonal skills needed to interact with potential research subjects
  • Ability to troubleshoot and problem solve
184

Research Coordinator Resume Examples & Samples

  • Monitors research processes to ensure data quality is in accordance with corporate standards
  • Verifies market analytical reports related to transactions, vacancy, development, absorption, rents, tenants, and leasing activity
  • Delivers statistical and analytical reports as required by leadership and sales professionals
  • Assists in training staff, management, and sales professionals in the use of research tools and resources
185

Research Coordinator Resume Examples & Samples

  • Responsible for coordination of a designated study or group of studies in a clinical or laboratory based research project. In clinical research projects, oversees recruitment of subjects, implementation of study procedures, and the collection, processing and analysis of data. In laboratory research, oversees and/or performs the scheduling of experiments, and the collection, processing and analysis of data and blood specimens. May be required to perform venipuncture on study participants
  • In clinical research, may ensure the safety and comfort of patients being evaluated; supervises the scheduling of patients for clinical and biological evaluations; sets up educational workshops for patients and families. In laboratory research, orders reagents and supplies as needed for experiments, schedules personnel, ensures access to research equipment
  • Administers and scores assessments such as functional disability ratings, side effects evaluations, neurocognitive measuring and/or other clinical ratings
  • Interfaces with the Research Grants Office; in clinical research with the Human Subjects Review Committee; and, as necessary in laboratory research, the Animal Care and Use Committee. In both clinical and laboratory research, organizes all phases of grant process for submission to funding agencies. Related responsibilities include the editing of manuscripts, grants and scientific articles and presentation
  • In clinical studies acts as liaison between the Federal Drug Administration and drug companies on related issues. Oversees availability of drug supplies and equipment for studies
  • Knowledge of Psychology, Basic Statistics and Research methods as normally acquired through completion of a Bachelor’s Degree in Psychology or related clinical field, required
  • Minimum of two (2) years progressively responsible related work experience to ensure working knowledge of research methods and analysis
  • Certified in Phlebotomy, required for venipuncture preferred
186

Research Coordinator Resume Examples & Samples

  • Demonstrated research administration experience and understanding of applicable principles
  • Working knowledge and understanding of programs and processes of primary granting agencies, to include, but not limited to, NIH and other federal, state and private foundation regulations and requirements, as well as corporate and private sponsors
  • Significant experience in office workflow management at the senior level with excellent organizational skills and the ability to change priorities quickly and often with little or no disruption to operations
  • Ability to work in a self-directed manner, demonstrate initiative and maintain a high degree of accuracy and attention to the smallest detail, with exceptional analytical and organizational skills
  • Working knowledge and understanding of an academic medical healthcare environment
  • Skill in program development and implementation; including and providing guidance in project management
  • Experience with planning, executing and evaluating programs, meetings and conferences successfully, including project management to include: developing project budgets; vendor selection; site selection; and, contracting
  • Ability to effectively communicate, with excellent oral and written communication skills
  • Experience with database systems. Demonstrated superior skills using Excel, Word and other Microsoft Office software applications
  • Experience developing and maintaining presentations and executive correspondences. Database management skills including the ability to create and query reports
  • Ability to gather, organize and maintain data and a proficiency in graphing, data-entry, spreadsheet, presentation software and other technical applications
  • Ability to work in a team environment, with demonstrated ability to work independently with limited supervision and ability to work toward common goals as part of a lager administrative team
  • Experience working within the University of Florida academic system is a plus, but not required
  • UF financial security clearance and ability to obtain VCU purchase card required
  • Must be able to interact with faculty, laboratory staff, students and visitors in a highly diverse environment – in person, via written communications, and on the telephone – with a high degree of professionalism
187

Research Coordinator Resume Examples & Samples

  • Manage and monitor all aspects of assigned projects. Including supervision of other research personnel supporting the project as needed
  • Coordinate and/or perform literature reviews and other information queries to assist faculty as needed to enhance their scholarly activity
  • Establish and maintain an understanding of and relationships of potential funding sources for specific projects and/or programs associated with the scholarly activities of the faculty
  • Other contract and grant duties as assigned by Director and/or PIs
188

Undergraduate Research Coordinator Resume Examples & Samples

  • 15% Enhance awareness about undergraduate research opportunities through courses, off and on campus events, workshops, etc
  • 10% Update undergraduate research program website and undergraduate research list serv on a regular basis
  • 10% Design and implement student outreach for undergraduate research opportunities and recruitment of students from groups traditionally under-represented in research. Serve as liaison to OSU academic advisors and faculty regarding promotion of undergraduate research
  • 10% Develop vision and strategy, in conjunction with academic units, committees and OSU leadership, for the promotion and expansion of undergraduate participation in research, scholarship and the arts as an integral component of OSU’s educational programs
  • 10% Pursue grant and other funding sources to support undergraduate participation in research
  • 10% Research and report on program activities as well as national trends and best practices in undergraduate research and experiential learning
189

Research Coordinator Resume Examples & Samples

  • May develop market research graphics for assigned specialty groups and gathers statistics and data from outside sources
  • If necessary, coordinates requests and responses between the local office and Company resources
  • Bachelor’s degree preferably in geography, urban planning, marketing, or business administration
  • Minimum of 1-2 year’s experience working in an office environment preferred
  • Familiarity with basic concepts of demographics and cartography
  • Strong organizational and multi-tasking skills
  • Strong PC skills in working with spreadsheets, database management and/or graphics packages
  • Strong initiative and self-reliance, ability to work independently
  • Ability to work various individuals at various levels of management
190

Senior Clinical Research Coordinator Resume Examples & Samples

  • Feasibility Assessment and Site Selection Process: Coordinate tour of facilities for sponsors
  • Site Initiation Process: Participate in sponsor-related site initiation visit. For PI initiated studies, assist PI in developing Site Initiation process
  • Enrollment of Patients: Identify patients for that meet criteria for protocol. Screen and consent patients for study
  • Treatment Phase: Provide clinical services as required including patient assessments, distribution of medications, collection of specimens, and timed blood collections (PKs). Appropriately document these encounters. Ensure that protocol-specific tests, scans, etc are scheduled and promote patient compliance to protocol regimen
  • Education of Patients: Educate patients about the study. Be available to answer patient’s questions and assist them when necessary
  • Adverse Events: Identify and access clinical adverse reactions and events. Notify appropriate parties of adverse events
  • Advocate for Patient: Advocate for patient’s well being
191

Senior Clinical Research Coordinator Resume Examples & Samples

  • Conducts clinical testing, develops protocols and assures all protocol procedures are approved
  • Bachelor's degree in sciences or related field. Master's degree preferred
  • 5 years of clinical research Excellent written and oral communication skills
  • Demonstrated leadership potential
192

OB / GYN Research Coordinator Resume Examples & Samples

  • Manages all aspects of conducting clinical trials
  • Act as liaison between the investigators, primary care providers, the Institutional Review Board (IRB), the Office of Clinical Research (OCR), and the sponsor
  • Along with the investigator, will screen, enroll and follow study subjects, ensuring protocol compliance and close monitoring while the subjects are on study
  • Responsible for all data and source documentation, adverse event reporting and maintenance of complete regulatory files
193

Research Coordinator Resume Examples & Samples

  • This position will serve as administrative and data support to the primary investigator, state project director, data and advisory groups
  • Excel knowledge and analysis is essential, the Coordinator will be responsible for analyzing data and developing charts/graphs for presentations
  • Manage communications for all stakeholders including meeting and communication updates, Website maintenance, branding and event planning
  • Assist in background research for the proposed quality improvement projects and support toolkit development for hospitals across IL
  • Be accountable for monitoring the safety and well being of all study participants
194

Research Coordinator Resume Examples & Samples

  • Bachelor’s degree in sustainability, environmental science, business or related field
  • Experience working with and reviewing technical materials
  • Experience interacting with technical staff
  • Experience driving projects to completion on time
  • Master’s degree in business administration, sustainability, environmental science, engineering, or related field
  • Experience leading meetings with technical staff both in person and via webinar
  • Experience managing projects with Microsoft SharePoint
  • Experience/knowledge regarding sustainability for consumer goods and supply chains
  • Experience coordinating technical projects between multiple locations, time zones and work schedules
  • Excellent communication skills both in person and via email
  • Ability to work with colleagues located in multiple offices
  • Ability to present processes and procedures to technical staff in Microsoft Powerpoint
  • Ability to understand and create technical content
  • Ability to communicate in an open and understanding manner
  • Ability to drive projects to completion on time
  • Ability to organize and analyze large amounts of information using Excel
195

Research Coordinator Resume Examples & Samples

  • Experience in research with knowledge about the conduct of clinical trials, research principles, and methodologies/study design
  • Bachelor’s degree in Health or Biological Sciences
  • Working knowledge of state and federal regulatory guidelines related to research
  • Good computer skills including working knowledge of a PC and Microsoft Office (Word, Access, and Excel)
  • Must be able to successfully pass the Basic Windows Skill Assessment at 80% or higher rating within 30 days of employment
  • Good communication, organization, and interpersonal skills
  • Good working relationships with colleagues, subordinates, and superiors
  • Develops, conducts, and facilitates research protocols
  • Supports investigators in writing study protocols
  • Performs participant screening, enrollment, study activities, and communication
  • Maintains equipment and supply resources for research studies
  • Obtains informed consent by following policy, procedure, and regulatory requirements
  • Schedules study-specific visits in conjunction with ancillary departments
  • Completes data management activities
  • Assists in the development and completion of source documents and case report forms
  • Completes data entry and ensures data integrity
  • Supports statistical services needs
  • Directs patient interaction to conduct research protocols
  • Completes research-only testing as required and applicable per study and system requirements, including electrocardiograms
  • Performs phlebotomy if trained to do so
  • Completes documentation as needed within the medical record
  • Monitors compliance throughout all study activities and engages compliance oversight as needed
  • Participates in education activities to support specific research activities and primary role at Children’s Healthcare of Atlanta
  • Maintains all licensure, certification, and system education requirements for role
  • Participates in educational activities related to study needs for study staff, investigator team, and patient care staff
  • Participates in departmental policy and quality projects
  • Manages all regulatory processes related to clinical research activities
  • Completes Institutional Review Board preparation, submission, modifications, reporting, and termination activities
  • Maintains all regulatory documents
  • Participates in sponsor correspondence, monitoring, and study meetings
  • Facilitates grants, contracts, and financial tasks for research and clinical trials
  • Supports Principal Investigator in study budgeting, sponsor interactions, routing, feasibility assessments, account management, and reconciliation
196

Senior Research Coordinator Resume Examples & Samples

  • 3 years of experience in clinical research with knowledge about the conduct of clinical trials, research principles, and methodologies/study design
  • Basic statistics
  • Self-motivated from a performance and professional development standpoint
  • Commitment to the lab’s and Children's Healthcare of Atlanta's missions, goals, and values
  • Broad knowledge of federal regulations and regulatory requirements for conducting research with the ability to mentor
  • Strives for good working relationships with colleagues, subordinates, and superiors
  • Develops, conducts, and facilitates research protocol at an expert level
  • Provides substantial support for investigators in writing study protocols
  • Leads participant screening, enrollment, study activities, and communication
  • Coordinates study visits and procedures, including specimen acquisition, transport, documentation, and shipment
  • Monitors process for services
  • Acquires equipment and supply resources for research studies
  • Provides leadership for data management activities
  • Develops and evaluates source and case report form tools
  • Manages data entry, ensures data integrity, supports statistical services needs, and collaborates with manager to assess data management needs
  • Provides leadership for direct patient care interaction
  • Completes research-only testing as required and applicable per-study and system requirements, including electrocardiograms
  • Coordinates educational activities related to study needs for study staff, investigator team, and patient care staff
  • Initiates departmental policy and quality projects
  • Provides leadership and training related to all regulatory processes related to clinical research activities
  • Ensures Institutional Review Board preparation, submission, modifications, reporting, and termination activities
  • Structures the maintenance of all regulatory documents
  • Leads others in sponsor correspondence, monitoring, and study meetings
  • Guides interdepartmental auditing of regulator practices
  • Independently provides services for investigators in study budgeting, sponsor interactions, routing, feasibility assessments, account management, and reconciliation
  • Serves as a collaborator and key contact for key business partners, including Emory, Georgia Tech, and University of Georgia
  • Works collaboratively with manager to monitor metrics
197

Research Coordinator Resume Examples & Samples

  • Knowledge in collecting heights, weights, behavioral, and physical activity data helpful
  • Ability to motivate parents and children to participate in the study and recommend it to family and friends
  • Fast learner, great organizational skills, resourceful, and capable of multi- tasking
  • Bilingual in Spanish and English is required
  • Must have a car or other ways of getting to community study sites around Houston, Texas, as work is performed at the Children’s Nutrition Research Center (CNRC) and various neighborhoods in Houston. Flexibility and adaptability in work schedule and carrying out job duties, including willingness to work some evening and weekend hours
  • Must be able to lift and move required assessment and physical activity equipment and materials. Ability to demonstrate fundamental movement skills and exercise to fathers and children
198

Sponsored Research Coordinator Resume Examples & Samples

  • Please include a cover letter in your application**
  • Provide general day-to-day operational support associated with activities related to incoming Federally sponsored grants and cooperative agreements
  • Prepare Budget Allocation Request (BAR) Forms for activation and modification of awards in Financial Management System, including, but not limited to restricted funding
  • Process Restricted Donation Awards (NDO’s)
  • Coordinate the Limited Applicant Award process
  • Within delegated authorities, exercises independent judgment in reviewing proposals, including, but not limited to a limited pool of non-competing subaward applications submitted by Fred Hutch staff for restricted funding
  • Manage monthly internal reporting and tracking processes, including, but not limited to the Pre-Expiration list process, and the Active without Award process, to ensure timely processing of activities
  • Assist in development and maintenance of tools to track monthly reports for management
  • May serve as primary contact on a limited portfolio assignment
  • Prepares journal vouchers and redistributions as needed
  • Serve as a resource for interpreting, explaining and applying Fred Hutch and sponsor policies, as well as applicable regulations related to research administration issues
  • Assist in resolving pre- and post-award issues related to sponsored projects
  • Advise Fred Hutch personnel and leadership of critical and/or sensitive issues related to sponsored projects administration
  • Represent OSR at institution-wide meetings and teleconferences, and attend professional meetings and conferences of research administration societies and associations, as applicable
  • Assist with special projects as assigned
  • Attend professional meetings and conferences of research administration societies and associations as applicable
199

Senior Clinical Research Coordinator Resume Examples & Samples

  • In collaboration with the Cardiovascular Institute physicians, obtains source documents (i.e. medical record documentation) as needed
  • Obtains consent and registers research participants with study sponsor (e.g. industry, NIH, etc.)
  • Maintains research record (e.g. patient consent, eligibility, case report forms (CRF), registration confirmation, corresponding source documents, etc.) for all patients enrolled in clinical trials
  • In collaboration with the physicians, completes and submits Serious/Unexpected Adverse Event Form for all internal and multicenter serious/unexpected adverse events as required by study sponsors, federal requirements and institutional guidelines
  • Actively participates in weekly Cardiovascular Institute meetings and conference calls (as applicable)
  • Maintains regulatory documents of epidemiology studies and clinical research databases
  • Communicates effectively with staff and outside agencies, and assists in the promotion of teamwork
200

Abcd Research Coordinator Resume Examples & Samples

  • Theoretical knowledge of psychiatry, psychology, or related field, and previous research experience in the related field
  • Bi-lingual, fluency in English and Spanish
  • Proficiency in using database software including Microsoft Office (Word, Access, Excel, and Power Point). Familiarity with using iPads and apps including Pearson/Q-Interactive, and NIH ToolBox. Experience using content collaboration software including Confluence and DropBox. Working knowledge of REDCap and E-Prime
  • Experience performing research duties in a clinical research environment and coordinating research studies. Experience with following a standardized multi-site Spanish and English research protocol in order to screen patients for eligibility, initiate study procedures, and collect data
  • Knowledge of MRI and Mock Scan procedures and MRI safety. Experience screening youth MRI subjects via the parent/legal guardian for MRI contraindications. Ability to maintain current MRI Safety Training and Certification through UCSD Keck Center for functional MRI and Mock Scan Training and Certification
  • Working knowledge of longitudinal research design and methodology and DSM V criteria
  • Experience administering detailed clinical interviews to youth and their parent/guardian including administering KSADS 5, demographic, mental health history, and experience asking minors about and documenting lifetime history of substance use
  • Knowledge of or experience in collecting biological specimens including saliva, hair, and urine samples according to a standardized protocol and following universal precautions
  • Understanding of IRB and NIH annual and unexpected reporting including enrollment, withdrawals, adverse events, and protocol deviations
  • Excellent planning and organizational skills and ability to work in a changing, multiple-demand setting in order to prioritize a large volume of work and meet deadlines efficiently and accurately
  • Bachelor's degree in psychology or social sciences
201

Research Coordinator Resume Examples & Samples

  • Background in nutrition, health science or related field
  • Fluency (spoken and written) in English
  • Requires meticulous attention to detail
  • General computer skills including working knowledge of Microsoft Office, and the ability to learn new software, systems, databases
  • Must be self-sufficient and able to identify problems and solve them
  • Able to work collaboratively in a small team
202

Senior Clinical Research Coordinator Resume Examples & Samples

  • Master’s Degree in a relevant health care field is required; plus two (2) or three (3) years of clinical research experience
  • Applicants possessing an RN or LPN license may substitute equivalent related experience such as clinical or clinical research experience
  • Equivalent experience, education and/or training may be substituted for the education requirements
  • Solid knowledge of computer software programs such as Excel®, Word®, and/or PPT
  • The ideal candidate will be detail oriented, have excellent organizational, communication and interpersonal skills, holds self accountable to high standards of professional excellence, be able to maximize resources and be resourceful, seeks and accepts personal and professional responsibility on a continued basis
203

Research Coordinator Resume Examples & Samples

  • Bachelor's Degree. Significant experience in research coordination can be substituted for education
  • Minimum one year experience in related field
  • Basic knowledge of FDA research policies, other applicable federal regulations and/or GCP guidelines
  • Well-versed in medical and scientific terminology
  • Familiar with medical records departments and information
204

Seasonal Background Check Research Coordinator Resume Examples & Samples

  • Conduct phone evaluations with candidates regarding information submitted on employment applications; Information would be including, but not limited to, criminal conviction history
  • Conduct phone evaluations with a high degree of accuracy, confidentiality and integrity
  • Maintain candidate focus to gather all information within the designated timeframe
  • Evaluate candidate responses to make an appropriate business decision while remaining compliant with all Federal, State, Local laws and EEOC and other agencies guidance’s relating to Employment background check policies
  • Prior Human Resources experience a plus, but not required
  • Ability to read, write and interpret instructional documents such as reports and procedure manuals
205

Research Coordinator Resume Examples & Samples

  • Excellent computer skills with knowledge of Access, MS Word, Excel, Outlook, PowerPoint
  • Meticulous organizational skills and proven ability to multi-task and work independently and
  • Demonstrated problem-solving ability and attention to detail while working in a fast-paced, deadline
206

Internship Research Coordinator Resume Examples & Samples

  • Experience with prospect and/or employer research
  • Experience working with CRM tools and systems
  • Experience managing data, including collection, entry, analysis, and reporting
  • Technical proficiency including Excel/mail merge/databases
  • Demonstrated skill with report writing and presentation of data
  • Demonstrated ability to provide high-quality customer service to staff, faculty, students & external partners and to collaborate across departments in a complex organization
  • Demonstrated commitment to principles of community and diversity, and the ability and desire to effectively and consistently relate to a diverse student population
  • Advising or mentoring experience is a plus
207

OPS Research Coordinator Resume Examples & Samples

  • Maintain participant records including informed consent and experimental procedures
  • Manage international media distribution via website monitoring and maintenance
  • Serve as liaison between university personnel and laboratory operations
  • Assist in manuscript preparation and submission
  • Assist with participant recruitment and scheduling
  • Assist in updating and maintaining laboratory website
  • Assist with planning and preparing visits from international scholars
  • Coordinate schedules and duties of laboratory research assistants and other personnel
  • Work with Center director and associated faculty on research-related needs
208

Research Coordinator Resume Examples & Samples

  • Manage the day-to-day operations of the research projects with investigators, consultants, data managers, study coordinators, outreach workers, and clinical staff
  • Coordinate all apects of the research projects with the study team
  • Hire, Train, and supervise 3 study coordinators, 1-2 outreach workers, student researchers, and volunteer staff
  • Work with the Principal Investigator (PI) to develop and update study protocols, including the development of new measures
  • Manage all Institutional Review Board (IRB)-related activities
  • Create regular reports for the IRB, funders (NIH and others) and PI
  • Coordinate meetings with study partners and represent study at clinical site meetings
  • Work with PI to develop recruitment strategies and manage tracking database; prepare weekly (and more frequent if needed) reports to PI about recruitment/tracking
  • Partner with IT/EPIC team and data programmers to modify and maintain study databases
  • Securely manage and maintain study data base
  • Perform regular audits to ensure that collected data are complete and accurate, and research protocols are being followed
  • Conduct research site visits to ensure that intervention is implemented as per protocol; maintain close communication with clinic champions along with study coordinators, conduct and supervise participant computer-assisted interviews
  • Extract and examine medical records
  • Assist in data analysis, drafting reports, preparing conference abstracts and presentations related to the project (e.g. posters, PowerPoint presentations)
  • Maintain and order study-related supplies
  • Maintain records of study incentives and travel reimbursements; facilitate other study-related financial transaction
  • Supervise, coordinate, and conduct data collection, data entry, and data management
  • Lead weekly project meetings
  • Supervise participant recruitment, tracking, and follow-up
  • Participate in disseminating study findings
  • Assist with preparationa dn writing of grant proposals
  • Troubleshoot study-related problems
  • Collaborate with Divisions Administrative staff to ensure execution of program budgets, subcontracts, consultant contracts and grant proposal submissions
  • Travel to clinical and research sites in the Bronx to oversee all study-related activities and facilitate participant recruitment and follow-up
  • Minimum Bachelor's degree required. Master's degree in Public Health, clinical epidemiology, or related field preferred
  • At least 3-5 years of experience managing research projects and staff
  • At least 3-5 years of experience collecting data for research (e.g. recruitment, conducting interview, extracting medical records and data analysis)
  • At least 2 years of experience working with a similar population
  • Advanced working knowledge of Microsoft Word, ACCESSm EXCEL, RedCap and SPSS (or SAS, STATA)
  • Ability to manage multiple priorities and projects while working as part of a geographically disbursed team, work with minimal supervision, and adhere to study protocol
  • Excellent interpersonal, organizational, and communication skills
  • Able to write scientific documents
  • Flexibility and willingness to work evenings and weekends are necessary
  • Fluency in English and Spanish required
209

Research Coordinator Resume Examples & Samples

  • Maintains and manages research databases of study participants, responsible for ensuring accuracy of data collection, data entry and adherence to established research guidelines
  • Conducts research interviews, screens subjects for participation in various research studies
  • Prepares Institutional Review Board applications and maintains regulatory documents for Institutional Review Board compliance for various research projects
  • Recruits research subjects and coordinates research visits. Meets with the participant and parent and/or guardian of the research participant to review and obtain consent for participation
  • May perform educational, developmental, or other forms of testing as required with research participants
  • Analyzes behavioral data, generates reports and builds queries
  • Assists with processing and analyzing neuroimaging data
  • Assists with planning and developing survey instruments
  • Participates in development of grant proposals and manuscript preparation including, but not limited to, conducting literature searches, performing data analyses, and assisting in the writing of manuscripts and grants
  • Orients students, research assistants and authorized visitors to the department and research protocols
  • Designs and conducts research experiments under the direction of the Associate Professor
  • Schedules and participates in research meetings
  • Must have 2 years’ experience coordinating investigator-initiated research protocols required
  • Some professional experience in a pediatric setting preferred
210

Research Coordinator Resume Examples & Samples

  • Collaborates with primary investigator, sponsor and research staff to plan, conduct and evaluate project protocols. Monitors and reports on progress of projects
  • Assists with the recruitment, selection, scheduling, and monitoring of research project participants. Manages the handling of adverse events, compliance and other participant-related issues
  • Collaborates to ensure compliance with applicable regulations and standards. Assists with responding to and preparing for audits
  • Manages clinical and regulatory compliance of the protocol including administration of study drug/device, adverse events/safety issues, medication interactions. May be required to respond to call
211

Senior Research Coordinator Resume Examples & Samples

  • Performs patient/family education about clinical trials as well as the research protocols. Ensures research needs are met at all family meetings (discuss progress of treatment, changes in therapy)
  • Acts as liaison between patient and physician concerning problems, adverse reactions, and other patient care issues, that may be related to the study
  • Follows-up with patients during each clinic visit to answer questions and assess for toxicities
  • Five years of relevant experience in a research or health care setting with Bachelor's degree or nine years of relevant experience in a research or health care setting without a Bachelor's degree
212

Research Coordinator Resume Examples & Samples

  • A minimum of 3 years of clinical operations experience, with increasing levels of responsibility. preferred to have clinical trials program management experience in Academia, Pharmaceutical, Biotechnology, Medical Device and/or CRO industry
  • Must have prior experience managing a clinical trial portfolio or large scale clinical trial program globally and be able to demonstrate a proven track record of successfully leading cross-functional projects in a global environment
  • Must have a thorough knowledge of clinical research concepts, practices, and FDA regulations and ICH/Good Clinical Practices regarding drug development phases, clinical research and data management methods
  • Therapeutic experience in infectious diseases preferred
  • Experience in early phase trials (Phase I-II) and First-In-Man trials is preferred
  • Ability to travel domestically and internationally is required
213

Research Coordinator Resume Examples & Samples

  • Three Years of relevant experience in a research or health care setting without a Bachelor degree. No experience required if candidate has a Bachelor degree in a related field
  • Excellent people skills
  • Complete all required training to conduct clinical research
214

Research Coordinator Supervisor Resume Examples & Samples

  • Supervises, hires, trains, disciplines and evaluates the performance of staff. Ensures performance appraisals are completed in a timely fashion
  • Provides technical and functional expertise in the area of Research studies. Recommends appropriate implementation plan. Monitors study routine to ensure progress of studies and reports to PI. Oversees compliance with regulatory and granting agencies
  • Makes recommendations for program enhancements, performance improvement, and "best practices."
  • Maintains comprehensive study lists for departmental information. Maintains cooperative relations with drug companies and other research centers for information on new research interests
  • Collaborates with PI and acts as a liaison between the Food and Drug Administration and drug companies on related issues. Adheres to and trains research staff on Good Clinical Practice, and regulatory and grant agency requirements. Keeps investigator informed of protocol changes or developments
  • Liaises with agencies including: IRB, OCG, pharmaceutical companies, laboratories, and equipment and supply companies as needed
  • Responsible for coordination of the day-to-day activities of the designated study or group of studies in clinical based research; ensures appropriate screening and oversees recruitment of subjects, implements study procedures, supervises the scheduling of experiments and the collection, processing and analysis of data
  • Ensures the safety and comfort of patients being evaluated. Supervises the scheduling of patients for clinical and biological evaluations; sets up educational workshops for patients and families; and provides on-call coverage for patient concerns/complications
  • Administers scores and evaluates assessments as assigned and as related to study protocol. Collects data, confers with PI and forwards results to sponsor (internal or external)
  • Interfaces with the Office of Grants and Contracts (OGC) and Institutional Review Board (IRB). Organizes all phases of grant process for submission to funding agencies as necessary
  • Bachelor's Degree, in a field of Science, Behavioral Science or related field, required
  • Minimum of three (3) years progressively responsible related work experience, including leadership, to ensure working knowledge of research methods and analysis
  • IRB Human Subject Protection training, required
  • Certification in venipuncture, electrocardiogram and vital signs, as needed per study protocols, required
  • Certified as a Clinical Research Professional, preferred
  • Excellent written and oral communication skills, required
215

Research Coordinator Resume Examples & Samples

  • Collaborate with investigators in the design, development, and documentation of data forms, questionnaires, and other survey materials
  • Responsible for aspects of the development of research recommendations and the design of research projects
  • Participate in the grant, manuscript, and Institutional Review Board process
  • Develop overall research plan for conducting surveys in the community
  • Conduct in-person or telephonic field research
  • Monitor selection and randomization process of study participants
  • Coordinate data collection of study participants, complete case report forms, and develop and maintain spreadsheets
  • Collect and maintain questionnaires and other data forms from study participants
  • Perform literature searches and write detailed written summaries of the findings
  • Collaborate with other project leaders on data presentation, interpretation and writing of scientific reports
  • Develop and maintain computerized data files for all data to be collected
  • May assist with budget /operational aspect of grant and contract proposals
  • Prepare summary reports and ongoing project evaluations for investigators
  • May help recruit, select, supervise and direct the activities of data collection employees and Research Technicians
  • Conduct quality control check on field data collection system
  • Collaborate with other research sites to insure consistency between research sites and accuracy of documentation
  • Bachelor’s degree in the sciences, health care, or equivalent experience
  • 1 year of related experience
  • Excellent organization, analytical, and interpersonal skills required
216

Research Coordinator Resume Examples & Samples

  • Provide support to projects through implementation of work plans, and preparation of deliverables. Assist in the documentation of project writing, preparation of material for project meetings and IRB submissions, summary reports, ongoing project evaluations, and coordinate arrangements applicable to assigned projects such as interview arrangements, etc
  • Administratively responsible for the clinical aspects of patient study subjects and testing
  • Participate in preparing project-specific data collection efforts including surveys, interviews, focus groups involving patients, state agency personnel and other key informants. Record and analyze pertinent data. Evaluate and update data in relation to protocol
  • Design and execute protocols and experiments, modify protocols as needed, and may be responsible for own research project
  • Oversee development of data collection instruments, survey tools and interview guides, perform and oversee data collection, management and analysis as necessary
  • Assist in writing the text of scientific publications and grants. Review literature
  • Assist in design, development and implementation of research endeavors for multiple principal investigators
  • Assist with the budget/operational aspects of the revenue and expense accounts. Compile expenses for fiscal reports and grant budgets. Assist grant accounting with grant reporting requirements
  • Responsible for maintaining all regulatory paperwork from study initiation, continuation, and termination (includes application for IRB, informed consents, HIPAA Authorization, etc.)
  • May help recruit, select, supervise and direct the activities of data collection employees, Research Technicians, and Research Coordinators
  • Comply with all safety and infection control standards appropriate to this position
  • Responsible for the inventory of research related supplies
  • 3 years of related experience
  • Demonstratedknowledge of federal requirements for the conduct of clinical trials
  • Experience in using computer based tools (Word, Excel, Access, Outlook, PowerPoint, etc.)
217

Senior Clinical Research Coordinator Resume Examples & Samples

  • Develop study protocols and data collection forms in collaboration with study investigators
  • Develop patient navigation intervention with investigators
  • Provide individual navigation to patients participating in the program
  • Work with senior level staff at health center sites to negotiate/implement/monitor research protocols
  • Train clinical research staff on the implementation of the intervention protocols, as well as the collection and documentation of data
  • Oversee adherence to project timelines
  • Coordinate Institutional Review Board (IRB) applications, continuing reviews, amendments, and files adverse events with the IRB
  • Plans, performs, and designs statistical analysis of findings
  • Set agendas for study team meetings
  • Serves as resource for patients during the course of the intervention
  • Performs reference searches in print and electronic media
  • Responsible for quality control and developing systems for QA/QC
  • Review data for quality assurance, descriptive statistics and manuscripts, as required
  • Assist with writing reports and manuscripts detailing research findings
  • Develops study budgets and assumes grant management responsibilities
  • High level time management and organizational skills
  • Ability to prepare and monitor budgets
  • Knowledge of current and developing research trends
  • Ability to meet the requirements of funding sources
  • Sound interpersonal skills and the ability to supervise others
  • Ability to identify problems and develop solutions
  • Ability to operate independently in a community health center setting and with good judgment
  • Proficiency of various software packages, including Microsoft Office, and other desktop tools
  • Ability to meet deadlines and work within budgets
  • Ability to compile data, analyze information, and produce reports
  • Bilingual in English and Spanish, preferred
218

Senior Clinical Research Coordinator Resume Examples & Samples

  • Nurses with 2 years of nursing experience may be considered for this position. The title and salary range of the position may vary depending on education level and any years of relevant research background**
  • Demonstrates a passion for developing others, enthusiastically and expertly precepts new hires during the orientation process, and serves continuously as a mentor. Analyzes clinical and behavioral situations, identifying learning opportunities to improve patient care and clinical research practices. Takes responsibility for identifying his or her ongoing professional development needs and independently seeks resources and opportunities to meet those needs, such as through membership in nursing, oncology, or research organizations. Regularly seeks feedback on performance and applies continuous professional improvement
  • Demonstrates productive working relationships internally and externally by taking accountability for actions, enthusiasm, motivation, commitment to patients and colleagues. Demonstrates an understanding of cultural differences and holds peers accountable for healthy relationships and maintains a conscious balance between work and personal life. Models safe work hours, time management and healthy lifestyle. AGE SPECIFIC COMPETENCY: The individual must be able to identify the patient's particular needs regarding age, education level, literacy and the presence of any language barriers so that all clinical research related instructions can be adapted to the patient's needs. This is particular important regarding the informed consent process. Must also be aware of the various institutional resources to facilitate this process. Note: The above statements are intended to describe the general nature and level of work being performed by people assigned this job. They are not exhaustive lists of all duties, responsibilities, knowledge, skills, abilities and working conditions associated with the job
  • Identifies opportunities to improve research practices and patient satisfaction by serving or leading teams as a change agent to launch innovations in patient care/satisfaction, clinical research, or supporting a healthy workforce. Actively participates in department or unit-specific quality improvement efforts. Identifies opportunity for quality improvement to colleagues and management
  • Provides an ongoing annual professional contribution: Ensures research documentation is comprehensive and facilitates protocol compliance; communication among colleagues; good clinical research practice; and patient safety. Utilizes a variety of strategies to enhance recruitment while being mindful of the needs of diverse patient populations and variables (fiscal and contractual) that affect clinical research. Practices solid communication skills, and is able to articulate and translate pertinent information. Creates a caring and compassionate experience by building healthy relationships with patients, families and colleagues
  • Serves as a role model of professional nursing practice as demonstrated by adherence to ethical practices during the conduct of clinical trials to protect the rights and well-being of patients and the collection of quality data. Consistently provides appropriate feedback to all members of the research team; participates in the peer review process; and utilizes multiple communication methods to facilitate the effective conduct of clinical trials. Demonstrates highly developed assessment and analytical skills within the context of clinical research by ensuring complete and accurate documentation to validate the integrity of trial conduct. Ensures the patient is initially and subsequently appropriately informed of protocol related/required procedures, expectations, and responsibilities as demonstrated by the documentation process of the Informed Consent
  • Minimum 2 years of nursing experience required
  • Minimum 2 years of research experience preferred, or required for Senior level
  • Annual completion of a VP approved professional contribution required for Senior level
  • Special Skills and Abilities Required Solid/Strong/Good or higher on most recent performance evaluation and maintain in practice Leadership abilities
  • Excellent role model
219

Senior Research Coordinator Resume Examples & Samples

  • Microsoft Office, ability to work with time-sensitive projects and write standard documents
  • Must be well organized with a keen attention to detail and able to multi-task
  • Must have excellent communication skills (both written and verbal) and the ability to analyze data/write/present
  • Spreadsheet, statistical analysis and data entry experience required as well as good customer service and patient care skills
  • Science and biology knowledge preferred
  • Patience and good customer service skills are critical as the patient population includes infants and children
  • Experience working with and troubleshooting computers preferred
220

Senior Clinical Research Coordinator Resume Examples & Samples

  • Assigns and oversees Assistant Clinical Research Coordinator duties on the assigned project
  • Responsible for monitoring volunteers’ compliance throughout the trial. Addresses day-to-day volunteer or study issues and escalates as appropriate
  • Prepares for and participates in sponsor/monitor/QA audits
  • Provides accurate and timely project status updates to Project Managers and sponsors
  • Ensures ongoing and timely communication with the Assistant Clinical Research Coordinator (ACRC) and other study team members
  • Actively participates or takes the lead with own team and others in process improvements, SOPs creation and/or revision, internal and external meetings and other team or company-related initiatives and goals
  • Serves as lead and main team liaison for common external vendors (local lab) and maintains and tracks these vendors
  • With or in the absence of management, provides guidance on study or team-related issues; supervises and provides feedback on clinic operations as required
  • Identifies training needs, establishes training materials and provides training within the team and others
  • With management and as required, assists in hiring and training of new staff and performance management of staff
221

Oncology Clinical Research Coordinator Resume Examples & Samples

  • Bachelor’s Degree in a relevant science or a related field (e.g. public health, health care administration) required
  • A minimum of one to three (1-3) years of research related experience, strong research specific knowledge base, solid knowledge of computer software programs such as Excel®, Word®, and/or Access®
  • The ideal candidate will be detail orientated, have excellent organizational, communication and interpersonal skills, hold self-accountable to high standards of professional excellence, be able to maximize resources and be resourceful, seeks and accepts personal and professional responsibility on a continued basis
  • Able to function independently and adjust hours to meet job demands
  • Association of Clinical Research Professional (ACRP) certification as a Clinical Research Coordinator (CRC) or Clinical Research Associate (CRA) or Society of Clinical Research Associates (SoCRA) certification as a Clinical Research Professional (CCRP) is preferred
222

Research Coordinator Resume Examples & Samples

  • Work with internal and external departments to understand research objectives and execute that plan as quickly and efficiently as possible
  • Run and maintain large scale count and quota tracking sheets
  • Assist with the development of tab plans as well as efficient visual ways of understanding the data
  • Run data requests using Decipher, STATA, R, or Survey/Reporter
  • Weekend, non-traditional business hours and some travel maybe required
  • BS/BA in Business, Marketing, Market Research or related field
  • 2 years’ experience in market research, consumer insights, brand management and/or strategy
  • Familiarity with quantitative research
  • Able to work autonomously
  • Possess the ability to identify gaps in process and documentation and take the lead on updating documentation
  • Ability to work on demanding projects with very tight timelines
223

Oncology Clinical Research Coordinator Resume Examples & Samples

  • Bachelor’s Degree in a relevant science or a related field (e.g. public health, healthcare administration)
  • Five (5) years of research related experience, strong research specific knowledge base, solid knowledge of computer software programs such as Excel®, Word®, and/or Access® required
  • Association of Clinical Research Professional (ACRP) certification as a Clinical Research Coordinator (CRC) or Clinical Research Associate (CRA) or Society of Clinical Research Associates (SoCRA) certification as a Clinical Research Professional (CCRP),is required
  • The ideal candidate will be detail orientated, have excellent organizational, communication and interpersonal skills, hold self accountable to high standards of professional excellence, be able to maximize resources and be resourceful, and seeks and accepts personal and professional responsibility on a continued basis
  • Equivalent experience, and/or training may be substituted for the education requirements
224

Research Coordinator Resume Examples & Samples

  • Coordinates day to day activities of research protocols which include screening, enrollment, and monitoring of research participants
  • Ensures accurate data collection, documentation, organization and safety of research participants
  • Interview, screen and recruit patients for study
  • Explains process and procedures to educate participant regarding the research study
  • Collects patient information
  • Process, document and enter information into a database
  • May perform Venipuncture (blood draws), EKGs/ECG’s and obtain vital signs on study participants
  • May collect, process, ship, and maintain paperwork for blood and/or biological specimens according to procedures outlined in study protocol
  • Employees may be required to receive on the job training of phlebotomy and EKGs/ECGs prior to performing on study participants
  • Maintains records and regulatory documents and records for research studies
  • Schedule research participant for tests and procedures, such as laboratory tests, x-rays, and other studies specific for the research protocol
  • Perform other job duties as assigned
225

Assistant Clinical Research Coordinator Resume Examples & Samples

  • HS graduation and sufficient experience and demonstrated skills to successfully perform the assigned duties and responsibilities
  • Proficiency with Microsoft Word, PowerPoint, and Windows
  • Excellent analytical and problem-solving skills
  • Ability to work effectively in a fast-paced, team-based environment; project management and coordination skills; ability to prioritize tasks and meet multiple deadlines on concurrent projects
  • Ability to establish cooperative working relationships with patients, co-workers, & physicians
  • Demonstrated proficiency with medical terminology
226

Assistant Clinical Research Coordinator Resume Examples & Samples

  • High School graduation or a General Education Diploma; and sufficient experience and demonstrated skills to successfully perform the assigned duties and responsibilities
  • Detail oriented, self-motivated and a record of exceptional performance meeting multiple deadlines for concurrent projects
  • Knowledge performing statistical analysis obtained through course study
  • Ability to analyze data using Matlab and other statistical software
227

Assistant Clinical Research Coordinator Resume Examples & Samples

  • HS degree or equivalent and six months to one year of related work experience
  • Proficiency with Microsoft Word, Excel, PowerPoint, and Windows
  • Demonstrated skills to successfully perform the assigned duties and responsibilities
  • Ability to exercise judgment and initiative
  • Must be detail oriented, self-motivated and able to meet multiple deadlines for projects
  • Ability to speak and write English
  • Statistical analysis background
228

Assistant Clinical Research Coordinator Resume Examples & Samples

  • Fluency in Cantonese language, verbally and in reading
  • Proficiency with Outlook, Excel, and Word, and experience with in database utilization
  • Ability to work with geriatric and cognitively impaired individuals
  • Fluency in Mandarin language (in addition to Cantonese, which is required)
  • Coursework in human or cognitive neuroscience
  • Experience administering cognitive tests
229

Assistant Clinical Research Coordinator Resume Examples & Samples

  • Working experience in Microsoft Word, Excel, PowerPoint, and experience with a statistical program such as STATA or SPSS
  • Abilities in conducting scientific literature searches and written summaries
  • Familiarity with scientific presentation and abilities in preparation of slides and reports
  • Ability to work respectfully with diverse communities to recruit young adult tobacco users for research
  • Outstanding communication skills both internal and external to the study team
  • Ability to identify problems, troubleshoot and propose solutions to the team
  • Demonstrated strong administrative and organizational skills
230

Assistant Clinical Research Coordinator Resume Examples & Samples

  • Bilingual in English and Cantonese and/or Mandarin
  • Must be comfortable, sensitive and operate within confidentiality standards with topics related to health and cancer
  • Travel within San Francisco required
  • Minimum one year prior experience working in healthcare related phone survey administration
  • Experience working in REDCap
231

Senior Clinical Research Coordinator Resume Examples & Samples

  • High school graduation or General Equivalency Diploma and three or more years of related work experience; or an equivalent combination of education and experience
  • In-depth knowledge of clinical research contracts and grants, clinical trials, protocols, FDA regulations, and complex visit structures
  • Financial analysis skills; demonstrated skills in preparing and presenting financial and quantitative analyses, including financial projections and budgets
  • Fluency in spreadsheet software; ability to develop and manage complex spreadsheets independently
  • Project management skills to oversee the administrative operations of the clinical trials program; knowledge of strategies for recruiting human subjects
  • Exceptional analytical skills to evaluate the importance and urgency of problems; excellent demonstrated interpersonal, verbal and written communication skills
  • Ability to analyze complex and non-routine issues requiring innovative solutions
  • Ability to operate effectively in a changing organizational and technological environment
  • Ability to assess and respond to audit risk; ability to develop project plans/schedules and motivate team to meet deadlines
  • Ability to interpret and apply policies and regulations
  • Certification by the Society of Clinical Research Associates or the Association of Clinical Research Professionals (within one year of hire)
  • Experience in risk management regarding study subjects, federal and non-federal sponsors and regulatory authorities
  • Experience with contract generation and subcontracting, preferably at UCSF
  • Experience using database software, such as MS Access or FileMaker Pro
232

Assistant Clinical Research Coordinator Resume Examples & Samples

  • Knowledge of patient confidentiality and HIPPA regulations (electronic and hard copy medical records, patient charts, communication, etc.)
  • Experience working with patients in a health care setting
  • Bachelor or Associate degree in health related field
  • Phlebotomy license (CPT1)
  • Bilingual (fluent in Spanish and English)
  • Ability to abstract data from electronic medical records (EPIC)
233

Assistant Clinical Research Coordinator Resume Examples & Samples

  • Fluency in English and Spanish Languages (written and spoken)
  • Proficiency in Microsoft Word, PowerPoint, and Windows
  • Bachelor’s or higher degree in Psychology, Neuroscience, Cognitive Science, or Biology
  • Experience and interest in elderly populations
  • Knowledge of CHR/IRB policy and procedure
  • Proficiency in data analyses software (SPSS, Stata, MatLab)
  • Willingness to perform administrative duties
234

Senior Clinical Research Coordinator Resume Examples & Samples

  • High school graduation or General Education Diploma and three or more years of related work experience; or an equivalent combination of education and experience
  • Significant project and clinical trial management experience or progressively responsible experience in a related position including regulatory and compliance responsibilities
  • Demonstrated ability to develop recruitment strategies in complex environments and differing patient pools, independently identifying recruitment leads, implementing new strategies, and continually adjusting strategies to meet current recruitment goals
  • Current certification by the Society of Clinical Research Associates or the Association of Clinical Research Professionals or ability to obtain within one year after hire
  • Good Clinical Practices (GCP) training
  • Current Basic Life Support Training (CPR) certificate
  • Prior experience in investigational drug clinical research (i.e. FDA clinical trials)
  • Fluency in spreadsheet software; ability to develop complex spreadsheets independently; demonstrated skills in audit preparation, execution, and follow-up
  • Experience in risk management regarding study subjects, federal and non-federal sponsors and regulating bodies
  • Experience with grant application procedures, personnel documentation, contract generation and subcontracting, preferably at UCSF
235

Research Coordinator Resume Examples & Samples

  • Plan, implement and monitor participant recruitment and retention procedures
  • Screen and interview study participants
  • Maintain case report forms, charts and documentation
  • Perform procedures as needed
  • Assists Division staff as needed
  • Job related travel as necessary
  • Writes status reports of current studies and updates departmental faculty on quarterly bases
  • Maintains database as requested by staff
  • Assists residents and fellows in research projects and the acquisition of data
  • Develop databases for the departmental staff
  • Assist staff in acquisition of IRB Applications
  • Maintains database on active IRB Studies for the department
  • Performs literature reviews as requested by staff
  • Maintains regulatory compliance and regulatory binders
  • Assists resident’s fellows and faculty in initial manuscript writing
  • Collaborate with study personnel in the strategic planning of future external funding grants
  • Develops research protocols that clearly describe research objectives and procedures necessary to test the hypotheses of the research project
  • Develop research designs, data collection methods and strategies for data management
  • Design, create and revise research instruments as necessary to ensure quality data that correlates with research objectives
  • Coordinates multiple data collection efforts for one or more research projects which may include other collaborating agencies or institutions
  • Consult with co-investigators on appropriate management of participant problems and concerns
  • Develop and manage interim reports for principal investigators, industry sponsors and institutional review board to ensure that each project is moving toward timely completion
  • Ensure that projects are executed successfully and completed within time frames to meet research objectives
  • Assists in preparation of all documents related to the informed consent process
  • Assists Principal Investigator in preparation and submission of informed consent documents to the appropriate departments
  • 2-5 years of nursing experience is preferred
236

Lead Clinical Research Coordinator Resume Examples & Samples

  • AA or BS degree in biological or clinical sciences
  • Previous hospital experience, experience abstracting or coding information from patient medical records
  • Laboratory skills for the safe operation of standard clinical centrifuge, separation of blood components, skilled handling of biohazardous material, pipeting, use of dry ice and liquid nitrogen for freezing and/or storing clinical samples
  • Effective oral and written communication skills
  • Skilled at chart review and abstracting data from patient charts
  • Skilled in finding and abstracting specific, required information from complex documents (e.g. Patient records, study protocols, etc.)
  • Competent in MS-Word and MS-Excel applications
  • Interpersonal skills necessary to work effectively with physicians, patients, nursing and ancillary staff in a variety of contact settings
  • Appropriate knowledge of anatomy, physiology, disease process and standard treatment protocols
  • Knowledge of Good Clinical Practice and ICH guidelines as adopted by the FDA
  • Working knowledge of Hospital research policies and procedures, HIPAA guidelines, IRB’s, and FDA regulatory requirements for clinical studies
  • Demonstrated maturity and capacity to maintain confidential information
  • Demonstrated ability to complete assigned tasks accurately and timely with appropriate training and supervision
  • Ability to take direction and to establish priorities, to self-direct and work independently
237

Research Coordinator Resume Examples & Samples

  • Assists with planning and staffing of project operations based on proposed research activities and timelines. Coordinates aspects of sponsor initiated and investigator-initiated research studies including subject recruitment, data collection, scheduling of study-related activities and follow-up of enrolled subjects. Provides guidance and direction to investigators, research personnel, and subjects. Assists with training and demonstrating techniques or procedures to less experienced research coordinators
  • Assists in recruiting subjects for studies and determines eligibility based on study criteria. Coordinates study participant activities including recruitment, screening, orientation and correspondence. Schedules subject appointments, tests, and procedures coordinating with external providers as needed. Produces reports, correspondence and other materials, as needed or required
  • Has responsibility for data collection for research studies following established data collection and management procedures. Collects, records, enters and prepares data for analysis. Performs basic study analysis under the direction of the Principal Investigator. Collects pertinent information from study participants through interviews, administration of tests or surveys or questionnaires, medical records review, or other collection procedures
238

Market Research Coordinator Resume Examples & Samples

  • Manage and optimize function space to ensure effective use of space
  • Analyze historical demand and create best practice scenarios to measure business opportunities against ideal date patterns, rooms to space ratio, food and beverage contributions and total revenue
  • Track and audit all space assignments on a daily basis
  • Maintain the Group Rooms Control Log (GRC)
  • Daily logging and distribution of definite and tentative bookings, cancellations, and revaluation’s
  • Generate the Weekly Sales Activity Report
  • Preparation and typing of the Advanced Sales Report/Director of Marketing Letter at the end of each month (to be in Corporate Office by the 3rd working day of the month)
  • Prepare and distribute monthly forecast
  • Generate 30-60-90 day forecasts as needed by the Director of Marketing and Director of Sales
  • Preparation and typing of Monthly Inventory Growth Analysis
  • Responsible for the OSCAR Program and it's parameters
  • Maintain a Kill file for Lead information
  • Maintain a Lost Business file
  • Distribution of Housing Pick-up Reports, Firm Rate Commitment Forms, and convention memoranda from Convention and Visitors Bureau
  • Aid the Director of Marketing and Director of Sales in monitoring the KRA benchmarks
  • Responsible to maintain monthly recap with reservations to insure GRC blocks is the same as Reservation blocks
  • Attend Weekly Sales Meetings
  • Assist Director of Marketing with coordination of special promotion mailings
  • Assist the office manager and the Director of Marketing in special projects
  • Bachelor’s Degree in Business or Hospitality Management is preferred
239

Assistant Clinical Research Coordinator Resume Examples & Samples

  • High School graduation and sufficient experience and demonstrated skills to successfully perform the assigned duties and responsibilities
  • Ability to work effectively in a fast-paced, team-based environment; ability to prioritize tasks and meet multiple deadlines on concurrent projects
  • Ability to establish cooperative working relationships with participants and co-workers
  • Demonstrated proficiency with research terminology
  • Experience working with participants in a research setting
  • Proficiency with statistical analysis software
240

Research Coordinator Resume Examples & Samples

  • Participate in preparation and writing of manuscripts, technical reports, formal presentations, and grant applications. Duties include preparing charts and tables, composing initial drafts, organizing and maintaining citations, doing data checks, and formatting documents following journal or grant guidelines
  • Assists with data collection and data entry of surveys and qualitative interviews. Assists in the coordination of project staff activities related to data collection. Assists PI and Faculty leadership in the supervision of data collection to ensure the project remains within the approved IRB protocol, as well as within timeline and budget concerns
  • Searches and organizes scientific literature using relevant databases and other sources (e.g., Medline and CSA databases); maintains bibliographical citation data using an appropriate software such as Endnote; prepares written summaries of literature
  • Master’s Degree with at least two years of experience in health-related research or quality evaluation
  • Attention to detail, particularly with regard to data accuracy and integrity
  • Strong computer skills (MS Office – including Word, Excel, PowerPoint, and Access)
  • Good working knowledge of data analysis software (e.g., SAS, SPSS or STATA)
  • Ability to handle protected health information and related human subject issues
  • Ability to travel to other locations within Florida for data collection and professional project meetings
  • Ability to interpret basic statistical results
  • Ability to work closely with PI and faculty to draft project proposals, manuscripts for publication in peer-review journals, and project reports
  • Ability to work independently, demonstrate initiative, and to collaborate with faculty and staff at multiple levels
  • Willingness to learn new skill sets and work in a cohesive team environment
241

Research Coordinator Resume Examples & Samples

  • Recruiting, screening, educating, and assisting potential study enrollees and their families throughout the length of the study
  • Obtaining informed consent
  • Scheduling research subjects’ appointments for tests and procedures
  • Responsibly handling and shipping biospecimens
  • Retrieving and submitting test results to appropriate party or data coordinating center
  • Entering study data from patients, families and medical records into a computerized database and/or on a case report form
  • Ensuring compliance with NIH and IRB regulations
  • Maintaining records and regulatory documents
  • Working effectively with a team of research coordinator to ensure appropriate and high-quality cross-coverage of different protocols
  • Participating in weekly project meetings
  • Helping meet study timelines as determined by the PI
  • Prefer fluent in Spanish and previous regulatory experience
242

AP Research Coordinator Resume Examples & Samples

  • Process payment approvals for utility, property tax, and loan invoices for all assigned associations, ensuring duplicates and other errors are corrected prior to check issuance
  • Team with property management to capture correct invoice information and to ensure processes are followed for timely payment of invoices to association vendors
  • Assist with ensuring proper workflows are established and maintained for routing of invoices through the approval process
  • Assist property management with proper coding of invoices to the general ledger
  • Troubleshoot issues in regards to invoices and payments
  • Provide training, guidance and support to system users in their information requirements, process management, and application knowledge; assist users on new processes and functions
  • Identify reoccurring errors and recommend training, documents and/or procedures to reduce errors
  • Research and respond to inquiries including, but not limited to, clarifying when an invoice will get paid, why an invoice was paid incorrectly and how to properly code an invoice
  • Research and resolve invoice issues related to unidentified properties, vendor issues, potential duplicate payments, image issues, missing invoices, missing payments, etc
  • Process the batching of approved invoices into the accounting system as well as resolve issues associated with this process
  • Support internal and external information requests
  • Resolve internal and external customer issues utilizing prompt, effective communication
  • Perform any range of special projects, tasks and other related duties as assigned
  • Three to five years of accounts payable experience
  • Must have strong computer proficiency and systems knowledge
  • Critical thinking, problem solving, good judgment and decision making abilities
  • Collaborative attitude and team player
  • Consistent professional demeanor
  • Work efficiently under pressure
  • Handle change in a positive manner
  • Reliable and discrete
  • Sitting at a desk for extended periods of time
  • Working at the computer throughout the day (keyboard and mouse use)
  • Ability to listen and focus for long periods of time
  • Ability to lift up to 30 lbs
243

Research Coordinator Resume Examples & Samples

  • 2) Excellent English writing and speaking skills are required
  • 3) Sufficient computer knowledge to interface with a variety of database, word processing, and scheduling
  • 4) Good communication and interpersonal skills
  • 5) Effectiveness in organizing tasks and setting priorities, multi-tasking, working efficiently with minimum oversight, interacting constructively with faculty and staff, and the ability to be adaptable, creative, and a quick learner
  • 6) Flexible working hours including evenings and weekends is essential
  • 3) Bilingual Spanish/English is a preferred
244

Mau-research Coordinator Resume Examples & Samples

  • Matches customer’s identified needs and criteria with available resources meeting minimum requirements of the department and expanding on this requirement to obtain personalised, confirmed, matched referrals or quick resources as appropriate
  • Creates, maintains and updates database with accurate information
  • Solves practical problems and interprets a variety of instructions furnished in written, oral, diagram, or schedule form
  • HSC and Diploma holder / Advanced Certificate in Management fields or Sociology or English or communication
  • Very good command of oral and written English and French
  • Very good telephone manner
  • Ability to work US/CA hours (from 17:00 pm to 02:00 am)
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Mau-research Coordinator, Working Hours Resume Examples & Samples

  • Conducts independent research utilising an existing pre-populated database, as well as other resources such as research files, Internet, archives, collections, print directories and zip code books
  • Participates and contributes to achieve team objectives and to be customer focus
  • Develops and maintains a strong professional relationship with the community of providers
  • Strives for continual improvement against personal development objectives
  • Develops and maintains ability to work on multiple search requests simultaneously involving different resources and level of expertise
  • Meets deadlines or exceeds the minimum required amount of searches per day. Prioritise daily caseload to ensure that all work is completed on time
  • Evaluates articles and/or resources to determine which are most appropriate to meet customer needs
  • Ability to read, analyse and interpret professional journals, detailed reports and general business correspondence
  • At least 2 years of experience in customer facing environment
  • Computer literate (Word, Excel, Outlook, Internet Explorer)
  • Typing skills and experience in proofreading and editing will be an advantage
  • Articulate, reliable and self-motivating
246

Research Coordinator Resume Examples & Samples

  • Draft IRB documents for the research studies, including original applications, submission of amendments, and annual reviews
  • Prevent IRB problems from arising
  • Troubleshoot IRB problems if they do arise. Maintain close contact by phone and in person as necessary with IRB staff
  • Perform basic data analysis. Assemble datasets from different sources, and prepare reports summarizing progress and problems in ongoing research studies
  • Build and maintain electronic data capture systems utilizing RedCap
  • Perform other research duties as required
  • Ability to prioritize a high volume of work under potentially high pressure to meet deadlines
  • Familiarity with medical terminology
  • Prior experience reviewing medical records
  • Familiarity with Word, Excel, PowerPoint, and data management programs
247

Research Coordinator Resume Examples & Samples

  • Acquires subjects for psychophysical/eye tracking experiments
  • Plans, schedules and conducts research experiments
  • Collects, compiles and analyzes data
  • Documents and interprets results of experiments and reports to supervisor
  • May develop and modify computer programs
  • Oversees the maintenance of lab equipment and environment
248

Research Coordinator Resume Examples & Samples

  • Assists Clinical Research Manager with pre-study visits and feasibility assessments
  • Completes case-report forms and performs quality assurance checks on all data (in coordination with the Q/QC Manager)
  • Coordinates regulatory and IRB interactions in collaboration with the ICTR regulatory staff
  • Recruits, screens, and enrolls research participants. Assists Principal Investigator with informed consent
  • Coordinates all treatments and tests with associated inpatient and outpatient facilities and staff
  • Follow-up with patients during each clinic visit to answer questions and assess for toxicities
  • Ability to travel between study site locations
249

Human Studies Research Coordinator Celebration Health Research Institute Celebration Resume Examples & Samples

  • BS in health-related field, OR
  • Bachelors degree in Science or Biology OR
  • 4 years experience coordinating research data and projects in the biomedical field
  • Specialized knowledge of the current internal and external regulatory needs of clinical trials
  • Personal qualities and interpersonal communication skills to interact and maintain good relationships with a broad spectrum of healthcare disciplines and the public under all circumstances
  • Detail oriented and teamwork skills
  • Motivated, organized, able to perform multiple tasks in a timely manner, and work efficiently under pressure
  • Ability to manage multiple clinical trials and function independently
  • Critical thinker and possess an analytical approach to problem solving
  • Ability to perform diverse administrative duties
  • Expert knowledge of Microsoft Office applications of Word, Excel, Access, Outlook, and Internet
  • Ability to adapt own approach according to investigator’s level of expertise to assure all institutional needs are met while learning occurs
  • Prior research experience (preferred)
  • Certificate from Clinical Research professional organization, i.e. SOCRA, ACRP (preferred)
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Assistant Clinical Research Coordinator Resume Examples & Samples

  • High School graduate with background in science and physiology
  • Experience working with a research group focused on disparities in the epidemiology or treatment of chronic conditions (i.e., hypertension)
  • Experience working directly with or research of low-income, safety-net patient populations and their healthcare providers
  • Excellent verbal and written communication and presentation skills; excellent organizational skills; and excellent interpersonal skills to work effectively in a diverse team
  • With guidance from supervisors and PIs ability to abstract data from medical records and transfer them to data collection forms or directly into databases
  • Experience working with clinical data to improve processes of care (i.e. data from chronic disease registries)