Study Coordinator Resume Samples
4.7
(99 votes) for
Study Coordinator Resume Samples
The Guide To Resume Tailoring
Guide the recruiter to the conclusion that you are the best candidate for the study coordinator job. It’s actually very simple. Tailor your resume by picking relevant responsibilities from the examples below and then add your accomplishments. This way, you can position yourself in the best way to get hired.
Craft your perfect resume by picking job responsibilities written by professional recruiters
Pick from the thousands of curated job responsibilities used by the leading companies
Tailor your resume & cover letter with wording that best fits for each job you apply
Resume Builder
Create a Resume in Minutes with Professional Resume Templates
CHOOSE THE BEST TEMPLATE
- Choose from 15 Leading Templates. No need to think about design details.
USE PRE-WRITTEN BULLET POINTS
- Select from thousands of pre-written bullet points.
SAVE YOUR DOCUMENTS IN PDF FILES
- Instantly download in PDF format or share a custom link.
AH
A Hickle
Adrien
Hickle
34679 Tanya Rapids
Philadelphia
PA
+1 (555) 691 1683
34679 Tanya Rapids
Philadelphia
PA
Phone
p
+1 (555) 691 1683
Experience
Experience
Houston, TX
Study Coordinator
Houston, TX
Hermann, Russel and Murphy
Houston, TX
Study Coordinator
- Manage and execute studies involving cohorts of genetically modified mice generated for studying embryonic stem cell biology and development
- Assist in measurement development, survey design, data management
- Assist with the hiring of staff and provide ongoing supervision of staff working in key areas
- Develops and update SOPs and other key study documents. Monitor the integrity of the procedures and data quality over time and implement quality improvement
- Assist the scientific staff with outline/protocol development, pre initiation meetings, and IACUC submissions
- Assists with procedures for data integration and efficient data management
- Assists with routine client visits as requested. Manages data transfer to clients as requested
San Francisco, CA
Regional Study Coordinator
San Francisco, CA
Marvin Group
San Francisco, CA
Regional Study Coordinator
- Provides overall management and execution of studies as assigned
- Monitor, track and provide resolution to all local study issues, keeping the Global Study Manager in the communication loop
- Monitor, track and provide resolution to all local studies issues and complaints, keeping the Global Study Manager in the communication loop
- Support a culture of continuous improvement, quality and productivity
- 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
- The fourth is mentoring and involving the right TMs in the village to assist in study execution
present
Los Angeles, CA
Study Coordinator Ii / Hours / Bwh Cci
Los Angeles, CA
Wilderman Inc
present
Los Angeles, CA
Study Coordinator Ii / Hours / Bwh Cci
present
- Participate in ongoing training and educational activities with CCI. Responsible for providing support for CCI program development
- Working in concert with Principal Investigator and/or Research Manager, develops and implements patient recruitment strategies
- Responsible for mailing various study information or packets to study participants
- Maintains inventory and orders supplies when necessary
- Interacts with patients/subjects with regard to the study, including patient education, procedural instruction, and follow-up. Serves as a liaison between patient and physician, and as a resource for participants and their families
- Communicates regularly with the PI(s) about all aspects of the research trial
- Meet regularly with Medical Director, Manager, and CCI Administration
Education
Education
Bachelor’s Degree in Initiative
Bachelor’s Degree in Initiative
Temple University
Bachelor’s Degree in Initiative
Skills
Skills
- Excellent communication and organizational skills
- Responsible for report preparation, including table and figure preparation. Compiles analytical information from laboratory groups
- Ability to work well in a team setting and independently is essential
- Ability to work in a team setting and independently is essential
- Ability to follow-up and ensure projects are completed in a timely fashion and within budget
- Outstanding judgment, initiative, and attention to detail
- Learns to serves as the primary contact in communication and interaction with other departments and clients as applicable
- Maintains well documented, organized, and up-to-date study files including study schedule, protocol, and correspondence, as applicable
- Responsible for report preparation, including table and figure preparation
- Serves as the primary contact in communication and interaction with other departments and clients as applicable
15 Study Coordinator resume templates
Read our complete resume writing guides
1
Biodefense GLP Study Coordinator Resume Examples & Samples
- Apply analytical biochemistry methodologies to support GLP studies
- Conceptualize and design detailed study plans
- Execute GLP studies as Study Director, as required
- Utilize techniques for immunoassay, cell culture assays and microbiology
- Tabulate, analyze and interpret data
- Assist with preparation of technical reports and manuscripts for publication
- B.S. in a biomedical science with at least 5 years of experience in biomedical research or equivalent experience
- M.S. in a biomedical science with at least 3 years of experience in biomedical research or equivalent experience
- Preference will be given to candidates with GLP experience
- Preference will be given to candidates with knowledge and experience in FDA regulatory affairs
- Must be able to enroll and maintain enrollment in the Biological Personal Reliability Program
- Must be a US citizen
2
Study Coordinator Resume Examples & Samples
- Team Management: budget decisions, hiring decisions, training and mentoring, delegating projects, forecasting staffing needs
- Coordinate literature review for the construction of various best practice guidelines for the American College of Occupational and Environmental Medicine. Advanced knowledge synthesizing medical literature and experience conducting exhaustive literature searches using various databases (PubMed etc.)
- Implementation and completion of multiple large population based epidemiological research studies
- Assist in establishing and accomplishing study objectives, ensure recruitment and follow-up of study participants throughout the course of the studies
- Apply statistical analyses (SAS preferred) to research projects for the purpose of effectively collecting and reporting data
- Plan and perform research in specified areas such as work related musculoskeletal injuries
- Write manuscripts and grants
3
Study Coordinator Resume Examples & Samples
- Assesses protocol for clarity and subject safety, reviews inclusion/exclusion criteria; clarifies concerns and questions with Principal Investigator and sponsor
- Attends and participates in Investigator and staff meetings. Advises team regarding specific study assignments and timelines
- Explains and obtains informed consent, medical history and demographics; documents in source file and maintains with historical data, status reports, progress notes, and subject log to help ensure subject safety
- Determines length of visits and coordinates related facility and equipment availability
- Reports and tracks adverse events (AE). Reports serious AEs to IRB and sponsor
- Documents all protocol deviations, reconciles test article accountability at study close out and prepares summary report for sponsor
- Completes, audits, corrects CRFs, relays CRFs to sponsor
- Maintains documents as required by FDA guidelines
- Maintains contact with IRB and prepares and submits IRB documents
- Ensures proper collection, processing and shipment of specimens
- Ensures uTRAC and any other University or departmental required tracking database is maintained
- Performs additional clinical research functions and assists resea
4
Study Coordinator Resume Examples & Samples
- Reviews protocol and inclusion/exclusion criteria, and screens and recruits eligible study participants; Monitors study enrollment goals and promotes enrollment and participant compliance
- Develops informed consent, source documents and screening materials
- Schedules and completes study visits; coordinates scheduling of protocol-required ancillary services
- Obtains informed consent
- Completes, audits and submits CRFs to sponsor
- Collects, processes and ships research samples
- Prepares, submits and maintains IRB, FDA, and other essential documents
- Ensures compliance with study protocols; manages quality control
- Recognizes, tracks and reports adverse events and protocol deviations per Institutional and federal guidelines
- Acts as a liaison between study site and Sponsor
- Prepares for and coordinates Sponsor site visits
- Attends and participates in Investigator and staff meetings
- Ensures uTRAC and other University or departmental required tracking databases are maintained
- Performs additional clinical research functions and assists research team members as required
5
Study Coordinator Resume Examples & Samples
- Recruit and assist PIs with focus groups, patient interviews, participant recruitment, participant surveys, and other study activities
- Data management, including validating patient samples, reviewing and updating information from paper and electronic records, and developing analytic datasets
- Coordinates day-to-day project activities, including tracking project requirements, scheduling investigator meetings, and generating meeting minutes
- Manuscript literature review, preparation, and editing
- Assists the Principal Investigators in the development of study protocols, manages human subjects requirements including IRB paperwork and procedures (new proposals, amendments, continuing reviews)
- Supervises, mentors and trains new or junior research staff
- Assists with grant writing activities
- Represents the research program at meetings and national and international research consortia
6
Study Coordinator Resume Examples & Samples
- Keep up to date with all certifications required to conduct Human Research projects,
- Assesses protocol for clarity and subject safety, reviews inclusion/exclusion criteria; clarifies concerns and questions with Principal Investigator or Study Lead, research team, and sponsor,
- Attends and participates in Investigator and staff meetings,
- Advises team regarding specific study assignments and timelines,
- Explains and obtains informed consent, medical history and demographics; documents in source file and maintains with historical data, status reports, progress notes, and subject log to help ensure subject safety,
- Performs observations and environmental sampling,
- Reports and tracks adverse events (AE) and reports serious AEs to IRB and sponsor,
- Documents all protocol deviations, reconciles test article accountability at study close out and prepares summary report for sponsor,
- Maintain contact with IRB and prepare and submit IRB-related documents,
- Coordinates the daily operations of assigned research team – coordinating the orderly and safe flow of the research project and maintaining adequate resources for the PI or Study Lead to accomplish research objectives of project,
- Other functions may include but is not limited to – grant writing, manuscript editing, data analysis, data organization, and literature searches
7
Study Coordinator Resume Examples & Samples
- Oversees compliance to protocol; manages quality control, completion and submission of study related documentation; prepares reports for organizations and agencies
- Disseminates information about the protocol to junior research staff
- Monitors enrollment goals and initiates strategies to promote enrollment and participant compliance. Coordinates and performs responsibilities related to research participants including determining subject population availability, developing informed consents and screening materials, screening and recruiting subjects, scheduling visits, obtaining informed consent, answering subject inquiries, overseeing study visits and acting as a liaison between participants and study-related parties
- Coordinate with data managers to monitor participant progression throughout study and conduct evaluation at end of study
- Recognizes, tracks and reports adverse events and protocol deviations
- Prepares for and coordinates site visits made by sponsors or federal agencies during the course of and at the close of the study
- Prepares, submits and maintains IRB, FDA, NCI, NIH, NSF and/or other regulatory documents and research correspondence
- Develops and maintains patient databases, investigational logs and records of drugs administered, medical devices monitored and/or procedures followed
- Completes ongoing training on techniques of clinical research coordination and practices, FDA Good Clinical Practices (GCP), and clinical research standard operating procedures to ensure compliance with policy and procedure, research sponsors and Federal rules and regulations
- Assures proper laboratory samples are collected and results reported to the proper entities
- Assists the Principal Investigator in the development of study materials
8
Reseach Study Coordinator Resume Examples & Samples
- Successful completion of a full 4-year course of study in an accredited college or university leading to a bachelor's or higher degree in a major such as social or health science or related; OR appropriate combination of education and experience and 2 years' research study or other relevant experience required; OR
- Strong interpersonal and communication skills, in-person and via phone/web
- Education in a field relevant to public health
9
Study Coordinator Resume Examples & Samples
- Implements and conducts stool specimen collections in clinical trials
- Implements and conducts a study with healthy individuals or individuals with polyps (SUPPORT Study)
- Implements protocol and assesses changes for compliance and subject safety, reviews inclusion/exclusion criteria, and clarifies concerns and questions with Principal Investigator
- Monitors budget expenses and billing for allied services
- Monitors enrollment goals and initiates strategies to promote enrollment and participate compliance. Coordinates and performs responsibilities related to research participants including determining patient eligibility, developing informed consents and screening materials, screening and recruiting subjects, scheduling visits, obtaining informed consent, answering subject inquiries, overseeing study visits and acting as a liaison between participants and study-related parties
- Prepares, submits and maintains IRB, FDA, NIH, NSF and/or other regulatory documents and research correspondence
- Contributes to developing educational materials and fundraising activities as part of the colon DOT
- Develops and maintains study participant databases and preforms some data entry activities
- Ensures proper collection, processing and shipment of specimens. Assists the Principal Investigator and Scientific Coordinator in the development of study protocols
- Assists with reports, scientific manuscripts, and grant writing
- Performs other responsibilities, including administrative tasks, as required
10
Study Coordinator Resume Examples & Samples
- Assesses protocol for clarity, reviews inclusion/exclusion criteria; clarifies concerns and questions with Principal Investigator and assists with participant recruitment plans and materials
- Advises research team regarding specific study assignments and timelines
- Determines length of visits and coordinates related facility and equipment availability for sponsor visits with PI and any requested study staff
- Completes, audits, corrects CRFs, relays CRFs to study team
11
Study Coordinator Resume Examples & Samples
- Adhere to IRB approved protocol
- Complete CITI training and adhere to GCP guidelines
- Develop and implement participant recruitment plans
- Communicate effectively with participants and colleagues
- Participate in the informed consent process
- Organize study documents and processes
- Data collection
- Case report form/Database completion
- Laboratory sample processing
- Schedule participants, providers, and team meetings
- Comply with Institutional policies and standard operating procedures
- Comply with federal, state, and sponsor policies
- Assist with essential document processing and IRB reviews
- Assist in monitoring and auditing procedures
12
Regional Study Coordinator Resume Examples & Samples
- Provides overall management and execution of studies as assigned
- Ensures DVA sites are committed to the project
- Helps project team to overcome organizational obstacles
- Accountable for the success of the studies, assists in selection and placement of clinical trials
- Leads study team
- Facilitates the team process
- 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
13
Study Coordinator, / Hours / Bwh Cci Resume Examples & Samples
- Initiates and maintains recruitment contact with study participants. Responsible for screening applicants, ensuring they meet appropriate criteria, and makes independent judgement as to the suitability of their participation. May be required to perform clinical tests such as phlebotomy, ECGs, etc
- Working in concert with Principal Investigator and/or Research Manager, and experienced coordinators to develop and implement patient recruitment strategies
- Working in conjunction with RCNet Manager and CCI Administrative Director on miscellaneous administrative duties integral to CCI/RCNet programs
- Interacts with patients/subjects with regard to the study, including patient education, procedural instruction, follow-up. Serves as a liaison between patient and physician, and as a resource for participants and their families
- In conjunction with Research Manager completed regulatory paperwork for institutional review board approval
- Answers phone calls and inquires regarding the study protocol. Refers participants when appropriate to principal and co-investigators
- Communicates regularly with the PI(s) about all aspects of the research trial
- Excellent interpersonal skills are required for working with the study participants
- Analytical skills and the ability to resolve technical or research problems and issues and to interpret the acceptability of data results
- Excellent organizational skills and ability to prioritize a variety of tasks
- Ability to demonstrate professionalism and respect for subjects rights and individual needs
- Knowledge of data management programs
14
Study Coordinator Resume Examples & Samples
- Participate in data 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
- Develop working relationships with project teams and advisory groups, fostering rapport, troubleshooting and problem-solving
- Resolve concerns relating to the research, taking direct action to address issues in a timely manner and/or bringing them to the attention of the supervisor
- Participate in study promotion, advertising, and outreach
15
Regional Study Coordinator Resume Examples & Samples
- Degree in Science or clinical degree with licensure preferred
- Competency Requirements
- Must be proficient with software including, Word, Excel, and Power Point. Microsoft Project a plus
- Customer service
- Conflict resolution
16
Study Coordinator Resume Examples & Samples
- Will work closely with all personnel involved in the research projects as well as study collaborators, which includes answering questions, scheduling appointments, and completing assessment visits
- Will be active in community recruitment of participants and continue to work with the participants throughout the project
- Explains and obtains informed consent; documents in source file and maintains with historical data, status reports, progress notes, and subject log to help ensure subject safety
- Will be responsible for developing, preparing and maintaining study materials, individual participant files, and the standard operating manual of procedures
- Will be responsible for data entry and perform basic data management tasks
- May compile research data and submit results to PI for including in publications, grants, and protocols
- May also interact with department administrative personnel and other departments on campus to ensure the efficient work of the projects and proper compliance with institutional policies
- Maintains accurate, detailed records and experimental data and protocols
- Reports and tracks adverse events (AE). Reports serious AEs to Research Manager and Principal Investigator
- Documents all protocol deviations, reconciles test article accountability at study close out and may assist in preparing summary report for sponsor
- May maintain contact with IRB and prepare and submit IRB documents
- May ensure proper collection, processing and shipment of specimens
- May perform functions required of the Clinical Research Assistant as necessary
- May prepare graphs, slides, and tables via computer to present findings of research projects to laboratory members during laboratory meetings
17
Study Coordinator Ii / Hours / Bwh Cci Resume Examples & Samples
- Coordinates the implementation, both internally and externally, of sponsored clinical research studies
- Initiates and maintains recruitment contact with study participants. Responsible for screening applicants, ensuring they meet appropriate criteria, and makes independent judgment as to the suitability of their participation. May be required to perform clinical tests such as phlebotomy, ECGs, etc
- Working in concert with Principal Investigator and/or Research Manager, develops and implements patient recruitment strategies
- Interacts with patients/subjects with regard to the study, including patient education, procedural instruction, and follow-up. Serves as a liaison between patient and physician, and as a resource for participants and their families
- Responsible for collection data and maintaining patient information databases for the study. Develops, organizes, and/or maintains the study forms. Responsible for data validation and quality control, data entry into CRFs, if applicable. May be required to input data, and do minimal analysis and run various reports
- In conjunction with Research Manager/Principal Investigator, develops and implements new research protocols including design, data collection systems and institutional review board approval
- Responsible for mailing various study information or packets to study participants
- Answers phone calls and inquire regarding the study protocol. Refers participants when appropriate to principal and co-investigators
- Ensure that knowledge about regulatory requirements are current by reading and attending local seminars related to policy and regulatory issues (FDA, NIH, IRB, etc.)
- Meet regularly with Medical Director, Manager, and CCI Administration
- Participate in ongoing training and educational activities with CCI. Responsible for providing support for CCI program development
- Monitors, maintains, sets up any study equipment
- Maintains inventory and orders supplies when necessary
- All other duties, as assigned
- BS OR BA
- 1 -3 years of work experience in clinical research, preferably actively coordinating research trials. Experience with Good Clinical Practice, CRFs, laboratory processes, safety practices, specimen shipping/handling, and study conduct
- Sound independent judgment and competence in research methodologies
- Knowledge of clinical research protocols
- Ability to demonstrate professionalism and respect for subject’s rights and individual needs
- Coordinator certification preferred
18
Field Study Coordinator Nairobi Resume Examples & Samples
- Assess the current use of the partograph and associated pain points of healthcare professionals
- Assess if the proposed DLDS solution can be used in different use cases (normal and/or abnormal labour and delivery scenarios)
- Work with the study team in preparation of study instruments and tools i.e. tablets, questionnaires etc
- Coordinate in the planning and conduct of participating health worker orientation meetings
- Work with the study team to ensure logistics for the activities are in order
- Provide logistical support and rapporteuring during orientation meetings and focus group discussions
- Coordinate the data collection activities at the facility, providing administrative, logistical and troubleshooting support in collaboration with the main study team
- Document accurate and comprehensive progress of study data collection activities at the health facility
- Conduct study tasks on other R&D project areas as assigned by the team leads and/or Head of Research, East Africa
- Weekly technical update reports to project lead
- Weekly logistics update reports to project lead
19
Glp Study Coordinator Resume Examples & Samples
- Coordination of non-GLP research and GLP preclinical studies conducted in-house and at Contract Research Organizations in laboratory rodents and large animals (including nonhuman primates)
- Ensure practices are compliant with FDA Good Laboratory Practice (GLP) and other federal, state and local regulations and guidelines (USDA, OLAW, AALAC)
- Scheduling activities for preclinical studies
- Receipt and communication of study updates, data, documents; ensure amendments and deviations are submitted within an appropriately defined time frame
- Ensure integrity of the data and the quality of all studies meets acceptable quality levels, to include tracking and storage of investigational materials and laboratory records
- Participating in the execution of laboratory animal studies by providing technical support and performing study specific procedures in the areas of anesthesia, procedures, pain management, and post-operative care as needed
- Facilitation of quotes and processing of invoices for approval
- Monitoring project timelines and milestones to ensure on-time delivery of projects
- Maintaining study protocols, outlines, and in-life data
- Organize, tabulate, and analyze data and laboratory records
- Coordination of receipt and handling of test article and study-related samples
- Maintenance of a Master Schedule
- Maintenance of electronic databases
- Developing, preparing and managing departmental standard operating procedures
- Preparation of final reports for IND filings and FDA submissions
- Assisting the Director in site visits and audits of contract facilities and vendors
20
Study Coordinator Resume Examples & Samples
- Assess study protocols for clarity and subject safety
- Review and understand inclusion/exclusion criteria
- Screen through schedules in EPIC for potential study participants and healthy control participants
- Determine length of visits and coordinate related facility and equipment availability
- Coordinate with study participants, clinics (within and outside the UU), physicians, and other research staff to schedule, create, and complete study visits
- Gather, record and enter data from study participants, charts, and EMRs into study databases
- Maintain source documents, status reports, progress notes, and subject logs in accordance with FDA guidelines, HIPAA, and GCP
- Report and track adverse events
- Document all protocol deviations, reconcile test article accountability at study close out and prepare summary report for department and sponsor
- Obtain and process biospecimens in accordance with protocols and good laboratory practices
- Assist in packaging and shipping of samples in accordance with IATA
- Perform QA as needed
- Clarify concerns and questions with Principal Investigator, laboratory manager, and sponsors
- Attend and participate in Investigator and research staff meetings
- Advise team regarding specific study assignments and timelines
- Will be required to work in a team environment as well as individually with minimal supervision
21
Associate Study Coordinator Resume Examples & Samples
- Ability to utilize word processing, databases, spreadsheets, and specialized software on personal computers
- Excellent communication, presentation, and interpersonal skills
- Ability to prioritize and manage time
22
Study Coordinator Resume Examples & Samples
- Consistently and continuously responds efficiently to requests (delivers high quality output on time)
- Contributes ideas and thoughts to enhance service and improve processes
- Provides constructive feedback to supervisor or team on study progress
- Follow instructions, SOPs and protocols that apply to current role to complete assigned tasks and projects
- Demonstrates ability and desire to learn and develop self
- Responds positively to requests for information and help from others
- Demonstrates a clear understanding of the need for working with individuals and in teams and contributes to the common goals of the business unit
- Ability to persevere and solve problems as they occur
- Demonstrates a positive attitude regarding challenging objectives
- Informs Study Director of any unforeseen circumstances that may affect the integrity of the study
- Works under supervision and guidance of more experienced colleagues
- Ability to utilise word processing, databases, spreadsheets, and specialised software on personal computers
- Skilled in the use of all standard laboratory equipment
23
Study Coordinator Resume Examples & Samples
- Bachelor degree in science plus one year of Study Coordinator experience. Relevant experience may be substituted for education
- Excellent interpersonal skills, as well as, service skills (internal and external) including attention to detail, accuracy, confidentiality and communication skills
- Skilled in concise writing. Writing should require little external review or edit
- Knowledge of grammar, punctuation, composition, and spelling according to company standard conventions
- Efficient use of word processing software, database, spreadsheet, and specialized software programs
- Efficient in managing time and prioritizing
- Knowledge of a variety of studies in the department and client base
- Knowledge of regulatory agency guidelines
24
Regional Study Coordinator Resume Examples & Samples
- Act as regional liaison between Global Study Manager and various CCLS departments involved in the study
- Act as regional liaison between assigned Client representatives (eg. CRA, Site Monitors) and the corresponding local CCLS platform; occasionally, the Regional Study Coordinator can represent Global Study Manager in interactions with the main client contact
- Close collaboration with the Global Study Manager for all study related aspects that are pertaining to the corresponding local platform and through all study stages, from set-up to closure
- Review the study Statement of Work to ensure local feasibility and make appropriate recommendations to the Study Design Lead
- Ensure a detailed knowledge of the SOW specifications and very good understanding of how the SOW specifications impact every operational aspect of the clinical trial
- Manage day-to-day local study related activities, especially logistics, monitoring and study supplies, keeping the Global Study Manager informed of any study development
- Monitor, track and provide resolution to all local studies issues and complaints, keeping the Global Study Manager in the communication loop
- Responsible for implementing monitoring and setting up of local performance metrics and taking corrective actions when needed
- Liaise with the Global Study Manager for any tasks assigned to the Regional Study Coordinator as part of the Global Monitoring Plan
- Demonstrate ability to work in a matrix environment where some task assignments are being channeled down to be dealt with by Regional Study Coordinators while other task assignments will need to be delegated by Regional Study Coordinators to other functional groups; demonstrate flexibility in handling both categories of tasks
- Participate in functional meetings (eg. CLFs) and provide input, keeping processes up to date
- Comply with CCLS Global Project Management strategy
- Support a culture of continuous improvement, quality and productivity
- 2 years customer service experience, preferable in pharmaceutical industry (Education may be substituted for experience)
25
Stability Study Coordinator Resume Examples & Samples
- Independently managing all aspects of a Stability Study from timeline and protocol development to final study report
- Developing and writing complete stability study protocols, interim and final reports
- Interacting with other team members and groups to coordinate all stages of internal and external testing, ensuring timeline milestones are met
- Reviewing stability study data for accuracy, trends and correlations
- Visualizing data for presentation to stakeholders at some routine frequency or upon request
- Bachelor’s degree in Biology, Chemistry or equivalent discipline
- Demonstrated project management experience required, project management certification preferred
- Understanding of ICH Guidelines related to Stability is preferred
- Experience in a cGMP environment and knowledge of cGMP requirements is preferred
- Experience with evaluation of analytical data including statistical analysis of stability data
- Ability to manage multiple products and timelines
26
Study Coordinator Resume Examples & Samples
- Implements clinical research protocols; clarifies concerns and questions with investigators and assists with participant recruitment plans and materials
- Conducts clinical study visits in coordinatation with other research staff
- Coordinates related facility and equipment availability for sponsor visits with PI and any requested study staff
- Works with study research staff as an effective team member
- Reports and tracks adverse events
- Maintains study documents as required by sponsor (NIH) and University guidelines
- Drives to study sites, including home visits
- Carries and transports study equipment and materials
27
Study Coordinator Resume Examples & Samples
- Education: Bachelor’s degree (BS/BA) or equivalent, preferably in a life science
- Experience: At least one year experience in a GLP laboratory environment preferred
- Other: Must possess high level of professionalism while interacting with all levels of staff and use sound judgment and diplomacy when communicating sensitive information. Must have ability to work in a multi-disciplinary team setting, ability to manage multiple priorities and projects and work under pressure with time constraints as well as meet departmental and company deadlines. Must have detail-oriented; organizational, writing, and proofreading skills. Intermediate to advanced word processing or database, spreadsheet experience required
28
Study Coordinator Resume Examples & Samples
- Works with Management to track study milestones and prepare monthly metrics
- Works with assigned Research Scientists to track study timelines on their projects and coordinate activities with other departments to meet study milestones
- Drafts/completes documents (protocols and reports)
- Assists in peer review of raw data files to ensure accuracy, conformance to SOPs, and completeness
- Performs minor corrections (e.g. addition of a study number, spelling correction) or corrects errors in raw data made by study personnel that may be unavailable but for which supporting information is available to justify the validity of the correction
- Assists with preparation/completion of results and summary tables, deviation
- Helps keep Sponsor, internal and external stakeholders (including Operations staff), group management, and WIL Research management up-to-date on progress of each study and copies group management on all correspondence. Notifies group management when trials fail, when timelines are behind, or when there are issues with a Sponsor
- Assists with follow-up training for Scientists and helps provides guidance to Scientists assigned on study-related aspects of the assay(s) and protocol requirements
- Performs method development and troubleshooting experiments for quantitative and immunogenicity assays with a progressive level of independence
- Works with Management and other groups to implement new processes/procedures, as required, to ensure that work is performed efficiently and in accordance with GLP regulations
- 3+ years of experience in a laboratory setting
29
Study Coordinator Resume Examples & Samples
- Serve as lead/primary technician on assigned studies to assure activities are performed in compliance with Good Laboratory Practices (GLPs), Standard Operating Procedures (SOPs), study protocols or Sponsor guidance documents and company policies/practices
- Read study protocols or Sponsor guidance documents and extract pertinent information related to required action items
- Assist the various stakeholders in the execution of study-related activities required
- Perform all tasks related to preparation and documentation of materials in support of sample collection, processing, management, and shipping. Includes entry of relevant information into LIMS systems or current database and may include scheduling shipments in the shipping database
- Review study protocols and provide recommendations to study director/supervisor on technical and logistical aspects of protocol design
- May work in conjunction with other departments to coordinate assignments to facilitate scheduling of study-related processes on assigned studies to ensure protocol or study requirements are met
- Prepare and review department calendars using protocols and other study documents to ensure all activities are appropriately scheduled
- Act as liaison between department staff, other departments, Study Director, Scientist and Study Supervisor on assigned studies
- May communicate with Sponsor representatives (e.g., the Sponsor, or third party laboratories subcontracted by Charles River Laboratories, SA or the Sponsor) on protocol-driven, study related activities conducted by Pathology Services (e.g., shipment of biological samples in support of assigned studies)
- Assist Study Coordinator II with study related activities
- Assure adequate and appropriate department study equipment and supplies are available for use on assigned studies
- Assist in preparing responses to both internal and external quality assurance audits
- Contribute to department process improvements and efficiencies in areas related to materials preparation, study samples, and study raw data to include SOP revisions, department inspections, and audits
- Serve as a model as it relates to effective time management, communication and utilization of resources, and safety in the laboratory. Perform a wide variety of laboratory tasks independently
- File and maintain data for department activities
- Maintain and perform record keeping
- Review data recorded by others for quality control
- Perform all tasks in compliance with Good Laboratory Practice Regulations (GLPs) and Standard Operating Procedures (SOPs)
- Education: High school diploma or General Education Degree (G.E.D.) required. Associate’s (A.A./A.S.) degree in a scientific field preferred
- Experience: Minimum of 3-5 years related experience, including GLP experience required, or must have demonstrated full knowledge of competencies and positive performance at the previous level
- Other: Good keyboarding skills, proficient in utilizing personal computer, e-mail and standard office software packages (word processing, spreadsheet, presentation, database). Ability to work on assignments that are extremely complex in nature where independent action and a high degree of initiative are required in resolving problems and developing recommendations. Acts independently to determine processes and procedures on new assignments and may provide guidance and oversee the activities of other support personnel
30
Study Coordinator Resume Examples & Samples
- Maintains study assignments and advises the study team on timelines for fellow and resident research projects
- Assists with negotiating contract budget and payment terms when appropriate
- May perform functions required of the Clinical Study Assistant as necessary
- Provides some departmental research support
31
Study Coordinator Resume Examples & Samples
- Enrolls eligible study participants; Monitors study enrollment and promotes participant compliance
- Ensures compliance with study protocols and applicable regulatory guidelines
- Schedules study visits
- Collects data from questionnaires and medical records and enters data into electronic data capture system
- Monitors and ensures data quality
- Collects, processes and ships research specimens
- Maintains essential documents files
- Attends and participates in staff meetings
- Performs additional research functions and assists research team as required
32
Study Coordinator Resume Examples & Samples
- Work experience (in healthcare, preferred)
- Clinical and/or Scientific experience in a research setting specifically with working with profiling
- At least 3 years of experience is preferred
33
Regional Study 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
34
Study Coordinator Resume Examples & Samples
- Learn to assist appropriate personnel in study set-up regarding study samples
- Learn to prepare or checks demographic import files and coordinates the preparation of tube labels
- Learn the process for ensuring the LIMS system is up to date with expected samples
- Independently drafts study documentation with some oversight, using an outline or client-supplied information. These documents includes protocols, sample analysis outlines (SAOs), amendments, study schedules, table and figures, and reports as applicable
- Maintains well documented, organized and up-to-date study files including study schedule, protocol and correspondence as applicable
- Proactively communicates and interacts with study team, other departments and clients as applicable
- Minimum of 2 years of study coordination experience
35
Study Coordinator Resume Examples & Samples
- Assists with developing procedures, milestones, and reports to support, monitor, and coordinate a wide variety of research projects. Establish and monitor benchmarks for each project
- Oversees the growth of a patient-centered network, including establishment of a registry and integration with electronic health record data
- Works with multiple stakeholders, faculty, and team members to coordinate multi-phased research and clinical projects
- Develops and update SOPs and other key study documents. Monitor the integrity of the procedures and data quality over time and implement quality improvement
- Oversees procedures for ensuring compliance with regulatory agencies
- Assists with procedures for data integration and efficient data management
- Assist with data analysis and report preparation for manuscripts, grant applications and interim monitoring reports
- Assist with the hiring of staff and provide ongoing supervision of staff working in key areas
- Assists with the development of grant applications and other proposals, analyzes project activities and prepares progress reports to the funding agencies and to relevant stakeholders
- 3+ years’ experience in managing clinical or epidemiological research projects
- Master’s degree in clinical effectiveness, epidemiology, biomedical engineering, or in a related field preferred
- Demonstrated teamwork abilities
- Expertise in database management and use of a variety of software for supporting research
- Understands research and clinical database structures
- Understands local and federal regulatory procedures for research
- Able to juggle multiple competing priorities in a fast-paced environment
- Be able to work independently with minimal supervision
- Excellent oral and writing skills
- Trains and orient new staff, in addition to hiring, terminating, evaluating and disciplining
- Coordinate staffing and scheduling
36
Study Coordinator Resume Examples & Samples
- Independently drafts protocols, sample analysis outlines (SAOs), amendments and study schedules as appropriate, using proposal outline or client-supplied information
- Reviews study compliance against protocol, SOP, and regulatory agency guidelines
- Learns to serves as the primary contact in communication and interaction with other departments and clients as applicable
- Updates and maintains project tracking systems as appropriate
- Responsible for report preparation, including table and figure preparation
- Maintains well documented, organized, and up-to-date study files including study schedule, protocol, and correspondence, as applicable
- Reviews client comments and makes decisions, including appropriate study personnel as necessary, to ensure that all necessary report/raw data clarifications are completed
- Responsible for report production through finalization, including archival of data as appropriate
- Assists with routine client visits as requested. Manages data transfer to clients as requested
- Assists SD/PI in monitoring study phases
37
Study Coordinator Resume Examples & Samples
- Explains and obtains informed consent, medical history and demographics; documents in source file and maintains historical data, status reports, progress notes, and subject log to help ensure subject safety
- Ability to locate funding opportunities both internal and external to the University. External searches will include foundations, federal, private, nonprofit, industry, etc
- Liaison with University offices to find and respond to all potential grant opportunities that PM&R faculty are interested in pursuing
- Maintain funding database for tracking all new internal/external funding opportunities, grants submission history, funds awarded, and grant reporting timelines
- Maintain communication with faculty about project interests and funding opportunities
- Participate in an interdisciplinary role with the division research team, faculty, rehab services and specialty teams
- Work collaboratively with Division administrative director, accountant and research manager regarding development of all budgets and ongoing financial management of active grant/projects
38
Study Coordinator Resume Examples & Samples
- Assists in the development of new report formats as needed
- Improves processes to increase the efficiency of daily/routine procedures and reporting methods
- Serves as the primary contact in communication and interaction with other departments and clients as applicable
- Participates in and assists Study Director/Principal Investigator (SD/PI) with pre-initiation and other study related meetings, including scheduling and leading meetings as required
- Prepares for and participates in routine client visits
- Manages data transfer to clients as requested
- Assists with training and mentoring less experienced staff
- Two years of Study Coordinator or related experience
- Efficient in prioritizing and managing time
39
Regional Study Coordinator Resume Examples & Samples
- Demonstrated ability to plan and prioritize
- Proven teamwork
- Demonstrated ability to facilitate meetings
- Demonstrated participation in process improvement initiatives
40
Study Coordinator Resume Examples & Samples
- Experience in school-based settings and/or working with school-aged children
- Evidence of a Masters degree in public health, nutrition, education, nursing, or related graduate degree
- Evidence of having credentials as a registered dietitian
41
Assistant Study Coordinator Resume Examples & Samples
- Graduation from high school or a General Education Diploma and two years of laboratory experience or two years of college including courses in the Psychology or related field and one year of laboratory experience, or an equivalent combination of education and experience
- Previous experience in a research setting involving human subjects including adolescents ages 12-21
- Experience in administering questionnaires to adolescents including Customary Drinking and Drug Use Record (CDDR), Hangover Symptom Scale, Family History Assessment Module, Youth Self Report/Adult Self Report, Pubertal Development Scale, Ten Item Personality Inventory, UPPS-P, Prosocial Tendencies Measure, Alcohol Expectancy Questionnaire, Adolescent Morningness-Eveningness Questionnaire, Beck Depression Inventory-II, Spielberger State-Trait Anxiety Inventory, and Karolinska Sleepiness Scale
- Experience in administering a battery of neuropsychological assessments according to the study protocol including WRAT 4 Arithmetic and Reading, Stroop Color Word, WebCNP, Delay Discounting, PASAT, Rey-Osterrieth Complex Figure, Grooved Pegboard, and WAIS-IV Digit Coding
- Familiarity administering to adolescents and/or parents/guardians structured diagnostic interviews including the SSAGA for youth and parent, and detailed questionnaires of substance use and mental health status
- Strong basic computer skills such as word processing and data entry, as well as experience using Microsoft Word, Excel, PowerPoint, and Access; RedCap; LimeSurvey; and AFNI
- Demonstrated experience and knowledge in assisting with neuroimaging data collection including setting up equipment, safety screening the participant, assisting operator in putting the subject in and out of scanner
- Experience in administering questionnaires to parents/legal guardians including Traumatic Brain Injury Identification Method, Access to Substances & Neighborhood Strength, Child Behavior Checklist, and Parental Monitoring
- Completion of UCSD MRI Safety Lecture and completion of annual on-line safety quiz to maintain certification status
- Completion of UCSD required Business Cash Handling training
42
Study Coordinator Resume Examples & Samples
- Assesses protocol for clarity and subject safety, reviews inclusion/exclusion criteria; clarifies concerns and questions with Principal Investigator, Project Manager, and sponsor
- Compiles and maintains research study Regulatory Binder as required by VHA research guidelines
- Assists with grant writing and other fundraising activities
- Oversees daily program operations and coordinates program activities
- Assists in preparing reports and manuscripts
- Prepares for and coordinates site visits made by sponsors or federal agencies during course and at the close of the study
- Contributes to developing educational materials and educates the community and other research professionals regarding studies and related research issues
- Assists the Principal Investigator and research staff in the development of study protocols
- Assist Project Manager with generating weekly project reports that are sent out to study team and presented at weekly team meetings. Compile agenda, take meeting minutes, distribute minutes for comment, send Outlook appointments
- Assist with searching and reviewing literature in pertinent areas and preparing written reports as necessary; copy, organize, and maintain journal articles
- May edit research papers, project reports, proposals and curriculum materials prior to publication or presentation
- Performs additional functions and assists research team members as required
43
Study Coordinator Resume Examples & Samples
- Study visits and follow-up
- Phlebotomy
- Review informed consent with patients
- Ensure protocol adherence
- Chart Review
- Recruiting patients
- Data entry and EDC management – DataLabs
- Any additional recruitment or study efforts deemed necessary by site
- MA/LPN/RN required
- Phlebotomy required
- Clinical trial experience required
- Orthopedic or spinal surgery experience desired
- Outgoing and willing to interact with many different people in a single day
44
Regional Study Coordinator Resume Examples & Samples
- Demonstrating compliance with good clinical practice (GCP) and applicable law, and verify that study teams comply with GCP and applicable law
- Demonstrating adherence to the DaVita Clinical Research (DCR) standard operating procedures and policies along with the standards customary in the clinical research industry
- Assisting the DCR project team in resolution of any challenges
- Accountable for the successful execution of clinical studies
- Participating in study site selection and placement of clinical studies
- Serving as a liaison between the physicians (Principal Investigator (PI) or Sub-Investigator), study sponsors and DaVita facility teammates (TM's)
- Support the study team to deliver or exceed project enrollment targets for clinical research studies at their site
- Responsible for accurate and timely data entry into the electronic data entry systems
- Responsible for timely resolution of all data queries to meet project timelines for database lock
- Understanding and promoting compliance with all applicable healthcare and research regulations
45
Cancer Prevention & Control Senior Study Coordinator Resume Examples & Samples
- Bachelor’s degree in health promotion, epidemiology or related field and two (2) years’ project coordination experience
- Experience in a research environment
- Experience with patient recruitment and consenting
- Experience with delivering educational interventions
- Experience working with multidisciplinary research teams
- Experience working with elementary and middle school children
- Experience with interviewing for medical research studies
- MS or MPH in epidemiology, public health, health evaluation or social sciences (or related field)
- Knowledge of epidemiologic research methods
- Collaborative work skills
- Ability to handle to handle and prioritize multiple tasks on tight deadlines
46
Study Coordinator Resume Examples & Samples
- Implements study in multiple clinics at HCI and is an effective team member
- Coordinates and performs responsibilities such as patient identification, recruitment, obtaining informed consent, and other patient communications
- Maintains information in patient databases and is responsible for data entry
- Helps support the ORIEN Avatar project
- Assists the Program Manager with HCI-Total Cancer Care research related tasks
- Works closely with the Biorepository and Molecular Pathology Shared Resource, multiple HCI-Total Cancer Care Working groups, and study PIs
- Monitors enrollment goals and helps to optimize the study
- Ensures proper collection and processing of specimens
47
Study Coordinator Resume Examples & Samples
- Manage and execute studies involving cohorts of genetically modified mice generated for studying embryonic stem cell biology and development
- Manage data collection, analysis and audits in studies to ensure that the data collected are complete and accurate, and that the research is being conducted as outlined in the study plan and protocol
- Work with the PI to develop and implement the study protocol and protocol amendments and develop appropriate progress reports for the PI
- Generate and characterize new mouse embryonic stem cell lines using standard tissue culture and cell biology techniques
- Organize and process mouse embryonic stem cell line database in the lab and record their characterization as outlined in study plan and protocols
- Partner with campus resource centers to enhance development of new protocols, databases and procedures for studies
- Facilitate the preparation of conference abstracts, oral presentations, and poster presentations, and participate in the development of manuscripts for publication
- Represent the study at internal and external academic meetings and community events. Act as a liaison to project partners to discuss new procedures that could be implemented
- Recruit, acclimate and supervise undergraduate and graduate student research interns. Supervise basic research trainees on a daily basis. Train staff and interns to collect and enter data appropriately
- Maintaining contacts with other members of the research team and collaborators on a daily basis
- Knowledge of basic molecular biology, standard tissue culture, cell biology and mouse genetics is highly desired/required
- Outstanding judgment, initiative, and attention to detail
- Ability to follow-up and ensure projects are completed in a timely fashion and within budget
- Ability to work in a team setting and independently is essential
48
Study Coordinator Resume Examples & Samples
- Responsible for tasks related to managing and recruitment of the Goals for Eating and Moving (GEM) study (oversees recruitment, manages participant flow, consenting participants) under supervision of the principal investigator
- Participate in the conceptualization, development, and implementation of the GEM research project
- Ensure adherence to study protocol and monitors quality control aspects of the study
- Coordinate and track all activities related to IRB (submissions, amendments, reports)
- Monitor goals and progress of the study
- Clean, code, and translate data; develop data dictionaries
- Assist with the successful implementation of intervention components. This includes health coaching patient participants both in-person and via telephone
- Assist in measurement development, survey design, data management
- Assist in developing, submitting and monitoring grant submissions
- Assist in the supervision of the non-managerial staff, e.g., interns
- Manage the grant budget related to the GEM study
- Assist in authorship and preparation of articles, abstracts, or presentations
- Minimum of 2 years’ experience with patients and/or in research
- Spanish speaking
- Strong administrative skills required
- Experienced with MS Office Word, Excel, and Access
- Data and project management experience a plus
- Data analysis experience (SPSS, SAS, or qualitative research analysis) a plus
- Worked in health care settings
- Experience working with diverse populations and patient populations
- Excellent interpersonal, writing, and communication skills
- Able commute to Manhattan for periodic team meetings
- Minimum commitment of 2 years
49
Study Coordinator Resume Examples & Samples
- Bachelor’s Degree. 1-2 years of related experience
- Biology/Science degree, prior research experience, and/or medical experience strongly preferred
- Priority given to candidates with Master’s Degrees
- Must be proficient in Microsoft Office and especially Microsoft Excel, and have the ability to apply technology to resolve problems
- Must be able to abstract data from complex medical charts in an efficient and timely manner
- Outstanding judgment, initiative, and attention to detail are essential. Must be able manage competing priorities while supporting the PI
- Can be relied upon to ensure that activities within areas of specific responsibility are completed in a timely manner and within budget
- Outline project goals and timelines and reviews progress at defined intervals
- Ability to work well in a team setting and independently is essential
50
Study Coordinator Resume Examples & Samples
- Oversees the recruitment, screening, scheduling, enrollment, interaction with, and consenting of subjects
- Monitors a large scale project (including scheduling and interacting with participants) and provides updates
- Coordinates with independent evaluators, interventionists, and clinicians
- Coordinates and schedules research participants’ study appointments
- Oversees the day-to-day activities of a clinical trial in accordance with Good Clinical Research Practice (GCP)
- Trains and supervises research staff on the proper procedures for conducting a clinical trial per GCP
- Prepares and submits materials for the Institutional Review Board (IRB) and other regulatory bodies as required by the protocol to ensure compliance in a timely fashion
- Assists with regulatory matters (such as data safety and monitoring and board meetings)
- Performs regular quality control assessments to ensure that clinical trial data is collected and stored per GCP
- Organizes and maintains documentation of participant and study data
- Manages data collection and databases
- May assist in the enrollment of human subjects
- May provide clerical and technical support to ensure adherence to research protocols and quality of information received
- Assists faculty by recording during data collection, data review and data entry, as appropriate for study protocol
- Interacts with co-workers, visitors, and other staff consistent with the values of Einstein
- BA or BS minimum
- Ability to work a Tues - Sat schedule (Saturday availability is a must)
- Database management experience
- Experience interacting with families of children with neurodevelopmental or related disorders (autism a plus)
- Management of clinical trials is a major plus
51
Study Coordinator Resume Examples & Samples
- Education requirements for the position: Bachelor's Degree
- Experience requirements for the position: 2-3 years
- Certifications, license or special trainings: Though not a requirement for this position, it would be an asset to the program if a candidate could be identified who has had prior experience working in clinical trials data management in either an academic or pharmaceutical setting and who understands the dynamics of such a position. Educational background that would be extremely beneficial includes clinical trials certification by SOCRA or other courses that provide this training
52
Study Coordinator Resume Examples & Samples
- Drafts protocols, and study scheduling, as appropriate, using proposal outline or client-supplied information
- Maintains template documents and standard method/procedure repository
- Reviews study data
- Communicates and interacts with various departments within, as well as, working in collaboration with clients
- Updates and maintains project tracking systems, as appropriate
- Responsible for report preparation, including table and figure preparation. Compiles analytical information from laboratory groups
- Participates in and assists Project Leader with pre-initiation and other study related meetings, as required
- Maintains well-documented, organized and up-to-date study folders/files including study schedules, protocol/report, and correspondence
- Reviews audits. Submits audit responses for approval, as appropriate. Follows up with appropriate personnel to ensure that all necessary report/raw data clarifications are completed within the specified time lines
- Reviews client comments and makes decisions, including appropriate study personnel as necessary, to ensure that all relevant report/raw data clarifications are completed
- Responsible for report productions through finalization, including archival of data as appropriate
- Assists with routine client visits, as requested
- Manages data transfer to clients, as requested
- Assists Project Leader in monitoring projects
- Assists with business administration/department metrics
- Bachelor degree in science or a program with an emphasis in writing (ex. English or Journalism) plus one year of related Study Coordinator experience. Relevant experience may be substituted for education
53
Study Coordinator Resume Examples & Samples
- Coordinate all scientific activities related to study conduct and schedule study activities with the management staff
- Assist the scientific staff with the preparation of data submissions and summary reports
- Assist the scientific staff with outline/protocol development, pre initiation meetings, and IACUC submissions
- Monitor studies in collaboration with scientific staff and in compliance with applicable regulations
- Coordinate study specific client site visits
- Maintain laboratory material inventories
- May assist in scheduling animal related activities and ordering animals
- Education: Associate’s degree (A.A./A.S.) or equivalent in life sciences or related field
- Experience: 4 to 6 years related laboratory animal experience
- Certification/Licensure:AALAS Certification preferred
- Other: Excellent written, verbal and organizational skills. Knowledge of SOPs and animal welfare regulations. Ability to interact appropriately with clients and all levels of employees and work effectively as a team member. Demonstrated abilities in analytical, quantitative and critical thinking. Proficient with computers and standard application software
54
Study Coordinator, Level Resume Examples & Samples
- Learns to manage increasingly complex projects and study designs and/or increased study load
- Assists in evaluating data for reports
- Reviews QAU report audits and submits audit responses for approval as appropriate
55
Study Coordinator Resume Examples & Samples
- Assesses protocol for clarity and subject safety, reviews inclusion/exclusion criteria. Clarifies concerns and questions with Principal Investigator and sponsor
- Maintains study assignments and ensures appropriate followup on study participants
- May perform functions required of the Clinical Study Assistant, as necessary
56
Regional Study Coordinator Resume Examples & Samples
- Act as regional liaison between Global Project Manager and various Covance departments involved in the study
- Act as regional liaison between assigned Client representatives (eg. CRA, Site Monitors) and the corresponding local Covance platform; occasionally, the Regional Study Coordinator can represent Global Project Manager in interactions with the main client contact
- Close collaboration with the Global Project Manager for all study related aspects that are pertaining to the corresponding local platform and through all study stages, from set-up to closure
- Manage day-to-day local study related activities, especially logistics, monitoring and study supplies, keeping the Global Project Manager informed of any study development
- Monitor, track and provide resolution to all local study issues, keeping the Global Study Manager in the communication loop
