Research Study Coordinator Resume Samples

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DW
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Dawn
Wiza
252 Kozey Drive
New York
NY
+1 (555) 604 6203
252 Kozey Drive
New York
NY
Phone
p +1 (555) 604 6203
Experience Experience
New York, NY
Research Study Coordinator
New York, NY
Carter LLC
New York, NY
Research Study Coordinator
  • Manages software development bug reports and communicate with project managers and technologists regarding issues in the field
  • Provide work direction & train other research staff regarding study technology and equipment
  • Assists in creating and editing study websites and databases; Assists in creating intervention mock ups and prototypes
  • Assist in developing research proposals
  • Lead and manage day-to-day operations of the Culture Collaboratory Lab, including extensive monitoring of undergraduate research students
  • Creates and maintains standard spreadsheets and/or databases
  • Assist in the preparation of human subject’s applications, consent forms and progress reports for institutional review board
Boston, MA
Clinical Research Study Coordinator
Boston, MA
Spinka-Emard
Boston, MA
Clinical Research Study Coordinator
  • Coordinates with Principal Investigator to help ensure that clinical research and related activities are performed in accordance with Federal regulations and sponsoring agency policies and procedures
  • Screens subjects for eligibility using protocol specific inclusion and exclusion criteria, documenting each potential participant’s eligibility or exclusion
  • Work on special projects as assigned
  • Development and/or maintenance of Standard Operating Procedures (SOP's)
  • Assists the Principal Investigator in submission of accurate and timely closeout documents
  • Establishes and organizes study files, including but not limited to, regulatory binders, study specific source documentation and other materials
  • Maintains adequate inventory of study supplies
present
Philadelphia, PA
Senior Research Study Coordinator
Philadelphia, PA
Pouros-Romaguera
present
Philadelphia, PA
Senior Research Study Coordinator
present
  • Performs physical function assessment
  • Participates in the planning & conduct of research studies
  • Participates in the planning and conduct of research studies
  • Administers tests and/or questionnaires following protocols
  • Administers tests &/or questionnaires following protocols
  • Codes qualitative data using NVivo software
  • Codes quantitative data using Stata statistical software
Education Education
Bachelor’s Degree in Related Field
Bachelor’s Degree in Related Field
Webster University
Bachelor’s Degree in Related Field
Skills Skills
  • Excellent organizational skills, including strong attention to detail and the ability to manage time effectively
  • Strong attention to detail and/or ability to follow and update procedural checklists/scripts
  • Strong proficiency with MS Office software (Word, Excel, PowerPoint)
  • Ability to work in a professional manner as both a self-starter and a team member
  • Able to complete assignments with attention to detail and high level of accuracy
  • Knowledge of English grammar and rules of composition, excellent verbal and written communication skills
  • Strong organizational skills and ability to multitask
  • Detail oriented with strong organization skills
  • Ability to explain complex information in a logical and simple manner
  • Skill/knowledge of medical testing output such as six minute walk test, spirometry, etc
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15 Research Study Coordinator resume templates

1

In House Clinical Research Study Coordinator Resume Examples & Samples

  • Recruit and schedule subjects for in-house studies which will entail communicating study objectives, inclusion and exclusion criteria, documenting informed consent and describing procedural expectations and restrictions
  • Prepare and conduct study procedures as outlined in an approved clinical protocol which will entail working with laboratory and clinical research personnel to obtain study supplies, applying or utilizing samples on various body parts, recording observations and data; and managing protocol deviations and adverse events
  • Create clinical study reports and collaborate with clinical research associate, statistician, and/or study requestor to finalize reports using software applications and eMatrix (applies to internal applicants) documentation system
  • Assist in the development and/or modification of clinical study protocols and clinical test methods including determining subject reimbursement and interacting with 3M ethics committee (Internal review board)
  • Operate laboratory equipment such as peel adhesion equipment, skin moisture meters, EKG monitors, electrode impedance meters and skin evaporimeters
  • Perform other duties as required such as maintaining and troubleshooting equipment; ordering laboratory supplies and training new personnel
  • High school diploma/GED or higher from an accredited institution
  • Combined experience in a laboratory and/or medical-related environment
  • Technical diploma or higher from an accredited institution
  • Experience as a Medical Assistant, Veterinary Technician, or certified Nursing Assistant
  • Microsoft Office proficient
  • Comfortable touching partially disrobed subjects during sample application and removal, and/or sample assessment and usage
2

Research Study Coordinator Resume Examples & Samples

  • At least two years of demonstrated research experience in a hospital/clinic setting
  • Previous computer experience including database management and/or development
  • Demonstrated experience with Human Subjects research
  • Demonstrated experience with Institutional Review Board applications and modifications
3

Research Study Coordinator Resume Examples & Samples

  • Lead and manage day-to-day operations of the Culture Collaboratory Lab, including extensive monitoring of undergraduate research students
  • Familiarity with SPSS, Qualtrics, and all Microsoft Office programs
  • Knowledge of Native American cultures and experience working with Native American tribes/communities
  • B.S. or B.A. degree related to Psychology
  • At least eight months experience working in a lab as a study coordinator or lab manager
  • Research interests aligned with the Culture Collaboratory Lab (e.g. racial ethnic minorities, first-generation college students)
4

Research Study Coordinator Resume Examples & Samples

  • Experience working with IRBs and obtaining consent
  • Experience with survey research,
  • Experience with REDCap
5

Research Study Coordinator Resume Examples & Samples

  • Strong organizational skills and ability to multitask
  • 1-2 years’ previous working experience coordinating clinical research trials
  • Skill/knowledge of medical testing output such as six minute walk test, spirometry, etc
6

Research Study Coordinator Resume Examples & Samples

  • Previous experience programming in Inquisit
  • Administration of the PPVT
  • Previous experience with Axis video systems
  • Previous experience working independently in a laboratory environment
  • Previous experience managing data and participants through Qualtrics Survey software
  • Skilled at Excel, Word, SPSS, and PowerPoint
  • Background working with gender nonconforming children and their parents
  • Previous experience supervising research assistants in a large, busy lab environment
  • Bachelor’s degree in psychology AND two years of experience as a Research Study Assistant (ideally also one year as a supervisor of other research assistants)
  • Six months of research experience in a lab working with gender nonconforming children
  • Background working with gender nonconforming children and their parents for at least one year
7

Senior Research 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 4 years' research study or other relevant experience required; OR
  • Two to four years of experience working in a team
  • Able to generate timelines for research activities that require participation from individuals in large teams
8

Research Study Coordinator Resume Examples & Samples

  • Aptitude for and interest in learning psychoacoustic and neuroimaging research methods that often involve complex equipment set- up and experimental paradigms
  • Strong attention to detail and/or ability to follow and update procedural checklists/scripts
  • Enjoy working in team environment and contributing to multiple projects
  • Ability to problem solve independently and work with minimal supervision
  • Familiarity with scientific research involving human subjects is preferred and familiarity with programming languages (especially Python) is desirable but not required
  • Interest in a long-term commitment to science
9

Research Study Coordinator Resume Examples & Samples

  • Evidence of excellent editing skills
  • At least 2 year experience with Second Life
  • At least 1 year experience working in the field HIV/AIDS
  • At least 2 year Experience with community based recruitment efforts
  • At least 6 months experience with programing surveys in RedCap, QDS, or Qualtrics or other similar interfaces
  • At least 1 year experience working with Microsoft Access databases
10

Research Study Coordinator Resume Examples & Samples

  • Must have general medical knowledge of dementia and other conditions commonly associated with older adults
  • Ability to be flexible, problem solve with creative solutions and work collaboratively to implement action plans
  • Current Driver’s License in good standing and access to reliable transportation
  • Experience in conducting qualitative interviews with diverse populations
  • Excellent interpersonal skills and ability to build rapport and trust quickly in new situations
  • Proficiency with Microsoft Office, Dropbox, and digital recording devices
  • Master’s Degree in Nursing, Social Work, Psychology or other related field
11

Senior Research Study Coordinator Resume Examples & Samples

  • Prior experience in the conduct of clinical research
  • Graduate level experience in a medical or life science related discipline
  • 2+ years conducting clinical trials
  • Familiarity with IRB, CT.gov, audits
12

Research Study Coordinator Resume Examples & Samples

  • Previous experience running research studies with child samples in experimental and clinical settings including obtaining child assent and parental consent
  • Previous experience conducting background literature searches in experimental developmental science
  • Previous experience with Excel, PowerPoint, and Word
  • Previous experience working training research assistants on lab protocols
  • Skilled at using SPSS for chi-square test, anovas, t-tests, and correlations
  • Background working with transgender children in research or clinical setting
  • Previous experience supervising or working with a large number of research assistants in a large, busy lab environment
  • Experience interviewing, recruiting, and screening participants for pediatric, clinical, or experimental studies
  • Bachelor’s degree in psychology AND one year of experience as a research assistant in developmental, pediatric, or clinical research lab with child participants
13

Research Study Coordinator Resume Examples & Samples

  • Excellent verbal communication skills
  • Experience recruiting and consenting subjects for clinical research studies.Experience using Study Tracker and REDCap
  • Health interview skills
14

Research Study Coordinator Resume Examples & Samples

  • Participates in the planning & conduct of research study including participant recruitment and retention; obtaining informed consent; administering tests &/or questionnaires following protocols; collecting, compiling, tabulating &/or processing responses; &/or gathering information. May extract & analyze data from medical charts. May complete basic clinical procedures such as drawing blood & obtaining blood pressure
  • 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 social or health science + 2 years experience; or 4 years practical research study or related experience; or a master's degree in a social or health science is required OR appropriate combination of education and experience.”
  • Experience interacting with human subjects and knowledge of IRB protocols
15

Research Study Coordinator Resume Examples & Samples

  • Knowledge of English grammar and rules of composition, excellent verbal and written communication skills
  • Master’s in Public Health with one year of experience working in behavioral science or biomedical research
  • Strong interest and experience in health promotion or disease prevention research
16

Research Study Coordinator Resume Examples & Samples

  • Experience working with Human Subject Clinical Trials
  • Training in Blood borne pathogens, CPR, Good Clinical Practices and HIPAA
  • Knowledge of FDA regulations
  • Demonstrates the ability to work independently as well as collaboratively as part of the team
  • Blood draw/phlebotomy experience
17

Clinical Research Study Coordinator Resume Examples & Samples

  • Coordinates with Principal Investigator to help ensure that clinical research and related activities are performed in accordance with Federal regulations and sponsoring agency policies and procedures
  • Prepares study materials to include, but are not limited to, the informed consent document, case report forms (CRFs), enrollment logs, and drug/device accountability logs
  • Establishes and organizes study files, including but not limited to, regulatory binders, study specific source documentation and other materials
  • Assists PI in communication of study requirements to all individuals involved in the study. Provides appropriate training and tools for study team members. Documents date of training and signatures of study personnel trained on study specific training log
  • Collects documents needed to initiate the study and submit to the sponsor (e.g., FDA Forms 1572, CVs, etc.)
  • Works with the PI to develop and implement recruitment strategies in accordance with IRB requirements and approvals
  • Conducts or participates in the informed consent process and discussions with research participants. Obtains appropriate signatures and dates on forms in appropriate places. Assures that amended consent forms are appropriately implemented and signed
  • Screens subjects for eligibility using protocol specific inclusion and exclusion criteria, documenting each potential participant’s eligibility or exclusion
  • Coordinate participant tests and procedures: including but not limited to preparing biological specimen(s) for storage and/or shipment to central laboratories as required by the study protocol
  • Collects data as required by the protocol. Assures timely completion of Case Report Forms
  • Maintains adequate inventory of study supplies
  • Completes study documentation and maintains study files in accordance with sponsor requirements and MetroWest Medical Center policies and procedures including, but not limited to, consent forms, source documentation, narrative notes if applicable, case report forms, and investigational material accountability forms
  • Maintains effective and ongoing communication with sponsor, research participants and PI during the course of the study
  • Assists Principal Investigator with scientific and compliance reporting requirements in accordance with Federal regulations and sponsoring agency policies and procedures
  • Assists the Principal Investigator in submission of accurate and timely closeout documents
  • Development and/or maintenance of Standard Operating Procedures (SOP's)
  • Work on special projects as assigned
  • Valid RN licensure within the State of Massachusetts
  • Professional research and healthcare experience desired
  • CPR certification required
  • Ability to prioritize among the assigned tasks
  • Ability to meet specific deadlines
  • Strong organizational, attention to detail and interpersonal skills
  • Ability to work as a team player with a high level of motivation and initiative
  • Experience with web based applications such as Meditech, Microsoft office, iMedidata, Oracle, Inform, Intralinks
18

Temporary Research Study Coordinator Resume Examples & Samples

  • Participates in the planning and conduct of research study including participant recruitment and retention
  • Obtains informed consent
  • Administers tests and/or questionnaires following protocols
  • Collects, compiles, tabulates and processes responses
  • Gathers information
  • Extracts and analyzes data from medical charts
  • Completes basic clinical procedures such as drawing blood and obtaining blood pressure
  • Enters data, identifies and corrects any missing data
  • Collects, records, reviews and summarizes research data
  • Collates relevant mathematical results and prepares tables, charts and graphs reflecting relationships of multiple tests
  • Prepares reports for investigators and sponsors on recruitment status and other pertinent study data
  • Writes portions of grant applications and co-author scientific papers
  • Completes documents associated with current local, state, and federal regulatory guidelines, requirements, laws and research protocols
  • Generates and circulates minutes from meetings
  • May process payments for research participants per study protocol
  • Coordinates reimbursements for expert panel travel, consultant pay, additional gift card orders, etc. and ensure costs remain within allotted grant budget
  • Successful completion of a full course of study in an accredited college or university leading to a master's or higher degree in a major such as social or health science or related; OR appropriate combination of education and experience
  • SPSS or SAS familiarity preferred
19

Research Study Coordinator Resume Examples & Samples

  • Computer Proficiency, especially Microsoft Word and Excel
  • Ability to coordinate study related activities with limited supervision under the general direction of the PI
  • Enhanced clinical understanding of the cardiovascular population
  • Familiarity with hospital electronic systems (i.e. electronic medical records, IDX, Cadence
20

Research Study Coordinator Resume Examples & Samples

  • Bachelor’s degree or higher in a field related to auditory or cognitive science (e.g., linguistics, audiology, psychology, health science, gerontology)
  • Experience conducting behavioral or educational research
  • Experience working with Institutional Review Board (IRB) requirements
  • Able to work independently with minimal guidance and as part of a team
  • Able to complete assignments with attention to detail and high level of accuracy
21

Senior Research Study Coordinator Resume Examples & Samples

  • Successful completion of a full course of study in an accredited college or university leading to a master'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
  • Neuropsychological test administration and scoring experience
  • Experience working with older adults
22

Research 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 social or health science + no experience or 2 years practical research study; OR appropriate combination of education and experience
  • Adaptability/flexibility
  • General understanding of accounting principles, experience with budgeting & financial management
23

Research Study Coordinator Resume Examples & Samples

  • Recruit, interview and screen potential subjects and determine eligibility according to established criteria
  • Run experiments in a lab, on-campus, on-line, and school settings
  • Collect pilot data in lab and on-campus
  • Determine and maintain quarterly lab schedules of experiments and research assistants
  • Consent human subjects and run them through study procedures
  • Interpret and record subject behaviors using observation codes
  • Record behavior of participants using sound and videotape equipment
  • Conduct subject interviews and record observations
  • Use statistical and database management programs to analyze data and prepare summary narrative reports, graphs, tables, charts and illustrations
  • Assist in the preparation of human subject’s applications, consent forms and progress reports for institutional review board
  • Perform related duties as required
  • Experience working with human subject divisions
  • Bachelor’s degree in psychology or a related field
  • Mature, organized, detailed-oriented and able to work independently
  • Ability to multi-task, have good problem-solving skills
  • Ability to communicate with all levels of project staff from student volunteers to scientists and PIs
24

Research Study Coordinator Resume Examples & Samples

  • Responsible for assisting the PI in recruiting subjects to participate in the study by using approved methodologies, such as, research out to healthcare providers and prevention coordinators for referrals, visiting clinics, sending mailouts, using approved advertisements, etc
  • Coordinates the enrollment of study participants, including explaining research procedures, and obtaining informed consent of subjects
  • Schedules appointments of study participants; conducts reminder phone calls and/or sends mailouts
  • Reviews the data collection forms, surveys and qualitative interview documents and recording, for each enrollee for completion and quality
  • Provides ongoing supervision of data collection activities
  • Obtains and distributes payment vouchers for participant reimbursements/participation
  • Perform administrative duties associated with the study’s Data Monitoring and Safety plan, tracking and reporting adverse events and collecting data specified by the DSMP. Responsible for all other administrative duties related to research activities
  • Prepares and maintains Institutional Review Board (IRB) approvals and correspondence, including amendments and renewals as necessary
  • Assist Investigators with manuscript and presentation preparation and research
  • Participates in staff meetings/initiatives including appropriate quality improvement activities, or if unable to attend non-mandatory activities, accepts responsibility to review meeting minutes and becomes knowledgeable of issues discussed
  • Conforms to hospital standards of performance and conduct, including those pertaining to patient rights, so that the best possible customer service and patient care may be provided
  • Utilizes hospital's behavioral standards as the basis for decision-making and to facilitate the hospital’s goals and mission
  • Follows established hospital infection control and safety procedures
  • Must adhere to all of BMC’s RESPECT behavioral standards
  • Previous experience with recruiting subjects, with an understanding of the ethical and technical conduct of research preferred
  • Experience with research administration, budgeting, IRB submissions, data management, and database development preferred
  • Excellent English communication skills (oral and written)
  • Cultural sensitivity and comfort with a wide range of social, racial and ethnic populations
  • Proficiency with Microsoft Office applications (i.e. MS Word, Excel, Access, PowerPoint, Outlook) and web browsers. Experience with statistical software a plus
  • Experience conducting interviews, coding, and analyzing qualitative data
  • Excellent organizational skills, including strong attention to detail and the ability to manage time effectively
  • Must be able to maintain strict confidentiality of all personal/health sensitive information
25

Senior Clinical Research Study Coordinator Resume Examples & Samples

  • Clinical research certification preferred
  • Driver's License
  • College graduate; Master's Degree in health care related field preferred
  • Must have knowledge of cancer and clinical protocols
  • At least three (3) years of experience in research program leadership
  • Three to five (3-5) years of sufficient health care experience in related clinical research and project management
  • Ability to create and conduct presentations to public and professional audiences
  • Ability to analyze and synthesize data, and prepare and present reports as necessary
  • Ability to maintain patient confidentiality
  • Ability to understand Federal regulations and translate those regulations to guide research work
  • Ability to facilitate and lead multi-disciplinary team of professionals involved in research studies
26

Research Study Coordinator Resume Examples & Samples

  • Understanding of clinical research components – data collection issues, human subjects protection, quality assurance and control
  • Familiarity with ICH Good Clinical Practices (GCP) consistent with registration clinical trials (FDA Guidance for Industry for Computerized Systems used in Clinical Trials (Title 21 CFR Part 11) preferred
  • Excellent programming ability in SAS statistical software is required. Knowledge of other programming and other scripting language is advantageous
  • Intermediate proficiency with Microsoft Office applications, use of file transfer protocols (FTP) preferred
  • Proficiency in a high level programming language preferred
  • Working knowledge of electronic data capture systems, specifically, Teleform (Autonomy Cardiff, Vista, CA) software preferred
  • Ability to learn and assimilate other related computer applications into data management practices
  • Demonstrated progressive work experience in project management and project planning
  • Great interpersonal skills and flexibility to work in a collaborative environment
  • Excellent organizational skills, including ability to multi-task, set priorities and meet timetables while managing several simultaneous projects
27

Resource Research Study Coordinator Resume Examples & Samples

  • Administer questionnaires
  • Enter computer data into file
  • Bachelor's degree (preferably in social, biological or healthcare sciences)
  • 6 months minimum experience as a research assistant in human subjects research (or equivalent position)
  • Experience facilitating recruitment and follow up strategies with clinic personnel and operational problem solving
28

Research Study Coordinator Resume Examples & Samples

  • Assist in identifying, recruiting and enrolling patients for clinical studies
  • Obtain informed consent
  • Obtain specimens
  • Be responsible and accountable for assessing, implementing and evaluating the delivery of subject/patient care while fulfilling the daily requirements of medical research protocols
  • Monitor the safety and well-being of all study participants
  • Bachelor's degree (preferably in social, biological or healthcare sciences) required
  • 6 months minimum experience as a research assistant in human subjects research (or equivalent position) required
  • Ability to interact in a professional and sensitive manner with medical personnel, research subjects, and other research staff
  • Must be able to work independently or with minimal supervision, and show initiative
29

Research Study Coordinator Resume Examples & Samples

  • Assist in identifying, recruiting, and enrolling patients for clinical studies
  • Be responsible and accountable for assessing, implementing, and evaluating the delivery of subject/patient care while fulfilling the daily requirements of medical research protocols
  • Previous experience in a research setting preferred
30

Research Study Coordinator Resume Examples & Samples

  • Working knowledge of Good Clinical Practices (GCP) and other state and federal regulations and laws
  • Active listening and coordination
  • Ability to coordinate 2 and more clinical trials with a minimal supervision
  • Master's degree in a social or health science and 1 year of experience in clinical research
  • Previous clinical experience in conducting clinical interviews with psychiatric population
  • Previous experience with diagnostic and symptomatology assessments commonly used in psychiatric research (i.e. SCID, M.I.N.I, PANSS, neurocognitive testing, side effects of drugs,.)
  • Conducting quality assurance and improving current standardized operational procedures (SOP)
  • Ability to to successfully coordinate 3 to 4 research projects or ability work on multiple protocols under a minimal supervision
31

Oncology Research Study Coordinator Resume Examples & Samples

  • Participates in initiation visits/investigator's meetings for assigned clinical trials (may involve travel) and implements these trials according to a deadline schedule mutually agreed upon by PI and sponsor
  • Develops study working folders for assigned protocols to outline guidelines for protocol compliance and to assure complete source documentation
  • Educates human subjects for participation in investigations. Educates clinic/hospital personnel for participation in protocol conduct, data collection process, and related conceptual issues as applicable
  • Coordinates the collection of data according to the research protocol, operations manual, and case report form guidelines within the budgetary guidelines established by the Clinical Research Manager
  • Directs the requisition, collection, labeling, storage, and shipment of specimens
  • Performs research related procedures (non-Standard of Care procedures) as directed by study protocol that do not require a licensed medical professional
  • Instructs Investigators on procedures and tests that need to be performed in compliance with the study protocol and advises Investigators on the results of procedures and tests; calling to attention findings of clinical importance
  • Documents research related examinations, procedures, tests, and other activities in appropriate clinic or hospital electronic medical records and/or source documents. Completes accurate and complete data entry into case report forms or pre-established electronic or paper data capture systems ensuring appropriate source documentation
  • Schedules follow-up visits for study patients in collaboration with Principal Investigator and provides source documentation for the activities conducted during these visits
  • Schedules and undergoes sponsor routine monitor visits and quality assurance audits for periodic reviewing and querying of collected data in a timely fashion
  • May be responsible for supervision of and delegation of work to clinical research staff
  • Duties performed may include one or more of the following core functions: (a) Directly interacting with or caring for patients; (b) Directly interacting with or caring for human-subjects research participants; (c) Regularly maintaining, modifying, releasing or similarly affecting patient records (including patient financial records); or (d) Regularly maintaining, modifying, releasing or similarly affecting human-subjects research records
32

Research Study Coordinator Resume Examples & Samples

  • Experience working on L&D
  • Experience in obstetric clinical studies
  • Experience handling biospecimen
  • Knowledge of basic obstetrical diagnoses
  • Ability to recruit patients for observational studies on L&D
  • Provision of informed consent
  • Ability to collect, safely handle, and process biospecimens
  • Knowledge of and ability to comply with institutional research policies and guidelines
  • Excellent verbal skills
  • Excellent multi-tasker
33

Research Study Coordinator Resume Examples & Samples

  • Must be bilingual/fluent in Spanish
  • Have an MPH or Master’s degree in social or health sciences
  • Have at least 1 year of research experience in social or health sciences
  • Knowledge of the scientific method
  • Experience with obtaining informed consent from study participants
  • Experience with data collection e.g., conducting surveys, semi-structured interviews, or focus groups
  • Strong proficiency with MS Office software (Word, Excel, PowerPoint)
  • Ability to work in a professional manner as both a self-starter and a team member
  • Excellent writing and interpersonal skills
  • Plans, organizes, and schedules in an efficient, productive manner
  • Anticipates contingencies and pays attention to detail
  • Takes initiative to solve research problems
  • Strong motivation to succeed as a member of our interdisciplinary research group
  • Institutional Review Board submission experience
  • Experience with recruiting and obtaining informed consent from research study participants
  • Experience collecting data from human subjects
  • Qualitative research and analysis experience
  • Experience with SPSS
  • Familiarity with chronic disease management
  • Good writing skills, publications
  • Survey research experience
  • Training in qualitative research methods
  • Experience with writing data reports
  • Qualitative data analysis software experience (e.g., The Ethnograph, Atlas TI)
  • Interest in chronic illness management, health care policy, and Veterans health
34

Research Study Coordinator Resume Examples & Samples

  • Obtains, extracts and reviews sensitive medical records data on identified subjects
  • Systematically inputs data into a specified form to be used for further analysis
  • Will need to be able to handle, manage and organize sensitive information in a secured and confidential manner
  • Faxing requests to clinics and facilities to obtain medical records information
  • Assist with data entry, data cleaning and maintenance of database systems
  • Experience in medical records review
35

Senior Research Study Coordinator Resume Examples & Samples

  • Experience with Microsoft Office (Word, Excel)
  • Experience with STATA software
  • Experience with NVivo software
36

Research Study Coordinator Resume Examples & Samples

  • Prepare computer-based and assessment materials and training protocols
  • Assist with preparing, reviewing, and modifying Human Subjects (IRB) forms
  • Prepare timely status reports and updates for the Investigators
  • Assist in modification of procedures for collecting and summarizing data; participate in the development of procedures for the design of measurement instruments and scoring systems
  • Coordinate and conduct recruitment and retention communications to participants, including mailings, phone calling, text messaging, and emails
  • Schedule participants, coordinate room assignments, and conduct lab- based study sessions with participants
  • Coordinate subject payments for participation
  • Maintain tracking database of study participants
  • Perform data entry and analyses as needed and assist in data cleaning procedures
  • Use statistical and/or database management programs to analyze data and prepare summary narrative reports, graphs, tables, charts and illustrations; assist in developing a computerized system for tracking study subjects; monitor data quality control to ensure adherence to study protocol
  • Assist in manuscript preparation and related activities
  • Assist in recruiting and coordinating undergraduate research assistants
  • Assist in project management/coordination of office support
  • Perform the duties of Research Study Assistant
  • May direct the work of assigned staff
  • Experience preparing human subjects applications and knowledge of NIH requirements relating to research involving human subjects
  • Experience with computer- and/or web-based data collection
  • Knowledge of implicit cognition literature and social psychology or developmental psychopathology methodology
  • Knowledge of college drinking literature
  • Experience with grant preparation and administration
37

Research Study Coordinator Resume Examples & Samples

  • 1+ years of experience working directly with the Yakima Nation
  • 2 years of experience with data collection, data reporting, and data entering
  • 2 years of experience coordinating community outreach activities
  • 3+ years of experience working directly with the Yakima Nation
38

Research Study Coordinator Resume Examples & Samples

  • Assist with study set up and management for two randomized controlled trials
  • Assist with submission and editing of IRB submissions
  • Assist with recruitment and training of clinical staff
  • Assist with programming on line study measures to be used for data collection
  • Organize and manage recruitment and retention of study participants
  • Conduct telephone screenings to determine eligibility of interested participants
  • Supervise and manage undergraduate research assistants
  • Develop and manage a computerized system for tracking study subjects
39

Research 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 degree in social or health science + 2 years’ experience; or 4 years’ practical research study or related experience; or a master's degree in a social or health science is required
  • Bachelors of Science degree in biomedical engineering or similar field, with working knowledge of biomedical signal processing
  • Experience and/or interest in MR image analysis is a plus
40

Research Study Coordinator Resume Examples & Samples

  • Candidates must have a strong clinical background
  • Three years of experience working with middle or high school age youth and families; experience working with foster caregivers preferred. Must have strong working knowledge of parenting skills
  • Experience working with families and caregivers participating in parenting programs
  • Experience working with people of varied cultural and socioeconomic backgrounds
  • Must be willing to telephone families in evenings and during weekends if needed
  • Excellent oral and written communication and problem solving skills
  • Excellent organizational skills and attention to detail
  • Computer experience including Microsoft Outlook, Word, Excel, and Access
41

Research 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 in a social or health science + 2 years experience; or 4 years practical research study or related experience
  • Bilingual (English/Spanish)
  • Ability to work well both independently on a self-directed basis and in a team environment
42

Research Study Coordinator Resume Examples & Samples

  • 2 or more years of relevant experience
  • Prior working experience administering surveys to diverse patient populations
  • Knowledge/ability to conduct and analyze qualitative and quantitative interviews
  • Knowledge/skill in utilizing Microsoft Office software, specifically Excel and PowerPoint
43

IHP Research Study Coordinator Resume Examples & Samples

  • 1) Recruiting participants
  • 2) Maintaining communication with families throughout the year
  • 3) Assisting with ERP data collection and analysis
  • 4) Training and providing technical support for lab personnel
  • 5) Additional responsibilities may include, but are not limited to: conducting literature reviews, maintaining IRB protocols, organizing and maintaining databases
  • 6) Perform other related duties incidental to the work described herein
44

Research Study Coordinator Resume Examples & Samples

  • Ability to recruit patients for observational obstetrical studies
  • Ability to collect research data from multiple platforms and enter into data system
  • Knowledge of grammar and rules of composition, excellent verbal and written communication skills
  • Critical thinking, active listening, persuasion, ability to express ideas so others will understand
  • Ability to problem solve, ability to multitask and ability to manage multiple priorities
  • Proficient in use of Microsoft Office products, including Word, Excel
  • Experience working in obstetrical studies
45

Research Study Coordinator Resume Examples & Samples

  • Microsoft Word, Excel, PowerPoint
  • 1 - 2 years’ previous working experience coordinating clinical research trials
  • Previous working experience with regulatory submissions involving an Institutional Review Boards (IRB)
  • Previous working experience with medical chart data abstraction
  • Previous working experience with basic medical evaluation skills, i.e. measuring blood pressure, pulse, body temperature
46

Clinical Research Study Coordinator Resume Examples & Samples

  • BA/BS degree in health sciences field
  • Experience working with patients
  • Experience working with clinical studies
  • Ability to organize and document clinical studies
47

Research Study Coordinator Resume Examples & Samples

  • Must complete Northwestern's IRB CITI training before interacting with any participants & must re-certify every 3 years
  • Must be bilingual (English/Spanish)
  • Prior Research Experience
  • Proficient with Microsoft Office
  • 5 years’ experience in community engaged research, and/or community engagement/community mobilization projects preferred
  • Knowledge and/or experience in public health, health literacy, medication adherence, or chronic conditions
48

Research Study Coordinator Resume Examples & Samples

  • Microsoft Office Excel, Microsoft Office Outlook, Microsoft Office Powerpoint, Microsoft Office WordMust complete NU's IRB CITI training before interacting with any participants and must re-certify every 3 years
  • Masters’ degree in public health
  • Prior working experience in behavioral science or biomedical research
  • Interest in organizational and public policy actions to prevent chronic diseases
  • Familiarity with basic statistical programming and descriptive analysis using SAS or STATA
  • Spoken fluency in Hindi
49

Research Study Coordinator Resume Examples & Samples

  • Detail oriented with strong organization skills
  • Ability to work independently and on a self-directed basis
  • Experience with EHRs/EMRs
  • Experience interacting professionally with medical practices and/or providers
50

Research Study Coordinator Resume Examples & Samples

  • A bachelor’s degree in a social or health science + 2 years practical research study; or 4 years practical research coordination or related experience is required
  • Must complete NU’s IRB CITI training before interacting with any participants & must re-certify every 3 years
  • Excellent computer skills with the ability to learn online web-based data collection, database management, data analysis techniques preferred
  • Data Management
  • BS or BA degree in psychology, public health, or related field, basic interviewing experience
  • One to three years of previous work experience in a clinical research environment
  • Experience conducting psychological assessments
  • Experience in hospital/academic research setting
  • Experience in HTML/CSS/JS/SQL
  • Ability to learn online web-based data collection, database management, and data analysis techniques
51

Research Study Coordinator Resume Examples & Samples

  • Proficiency in Microsoft officeapplications, including Excel and Powerpoint
  • Ability to manage multiple cases and projects at the same time
  • Experience recruiting and consenting subjects for clinical research studies
  • Experience using Study Tracker and REDCap
  • Experience interacting with clinical personnel
  • Experience with submission of research protocols, revisions, developing consent forms and management of IRB processes
  • Ability to explain complex information in a logical and simple manner