Research Coordinator Resume Samples

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Research Coordinators supervise and motivate team members and make sure projects are completed in due time. Work activities usually mentioned on Research Coordinator resume samples include developing plans, implementing methodologies, analyzing test parameters, writing reports, and presenting research findings to management. Those interested in a Research Coordinator job should showcase in their resumes research background, analytical thinking, attention to details, leadership, managerial skills and computer competencies. Employers select candidates holding a graduate degree in a relevant study area.

For more information on what it takes to be a Research Coordinator, check out our complete Research Coordinator Job Description .

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1

Research Coordinator

Coordinated internal Healthy Start Evaluation between academic partner, health centers, and volunteers

  • Created analyses of demographic and programmatic data for Healthy Start
  • Managed Registration for 1st Annual Healthy Start Community Conference
  • Coordinated Community Organizing Training for 6 local CBOs and community residents
  • Facilitated focus group on Research Interests for community stakeholders
  • Coordinated development team and submitted multiple grant proposals, including two proposals with Cook County Department of Public Health
  • Wrote needs assessment included in funded 2014 Healthy Start grant
Candidate Info
2
years in
workforce
1
year
at this job
BA
Political Science
2

National Institute of Health Clinical Research Coordinator

Evaluated, scheduled, recruited, and enrolled 10-18 year old patients and families of a community based clinic into a national clinical trial on vitamin D and the benefits on the cardiovascular health system

  • Effectively communicated with families, providers, and medical staff to efficiently coordinate study procedures set forth the by NIH protocol.
  • Cooperated with other health related agencies and organizations in community activities.
  • Assisted in the design an execution of programs that contributed to a 32% growth of the trial within 1 fiscal year.
Candidate Info
12
years in
workforce
2
years
at this job
BA
Psychology, And Spanish
3

Research Coordinator

Collaborated on a CDC funded research study evaluating an intervention using health resources and education with community partners for young men in Baltimore City

  • Managed evaluation data collection in seven Baltimore City health clinics
  • Establish and maintained relationships with health clinic leadership and staff
  • Managed and recruited 10 research assistance including hiring, training and scheduling
  • Developed standard operating procedures and documentation
  • Collaborated with the study leadership and attended weekly planning and update meetings
  • Conducted data cleaning and compiled reports
  • Conducted informed consent and participant interviews
Candidate Info
9
years in
workforce
1
year
at this job
C
Nursing
MA
Epidemiology And International Health
MS
Nursing
4

Regulatory Affairs/ Research Coordinator

Provide the highest quality patient care. This includes scheduling patients, creating charts, processing patient visits, completing visit forms and tests, performing ECG's, taking patient vital signs, entering data, and distributing medications.

  • Prepare clearly written regulatory reports. Maintain FDA regulatory compliance and obey clinical regulations of major drug company sponsors. Created and implemented dozens of Standard-Operating-Procedures to ensure compliance with regulatory standards.
  • Ensure quality, consistency, and accuracy in the conduct of clinical research trials.
  • Expanded the number of drug company studies.
  • Provided patient care to the maximum number of clients, increasing company revenue.
  • Achieved FDA regulatory compliance.
Candidate Info
18
years in
workforce
2
years
at this job
5

Senior Research Coordinator

Reliably responsible for organizing and maintain all aspects of many, multi-million dollar research studies both industry sponsored and federally sponsored with daily professional interaction with upper level administration, patients, families, researchers, nurses, and physicians.

  • Successfully met every recruitment goal resulting in 100% of all studies either closing on time, or earlier than predicted.
  • Effectively created training, marketing, and communication tools.
  • Devised and maintained Clinical Trials Center website to advance knowledge and relationships within the research field.
  • Initiate and produce study budgets generating increased revenues.
  • Publication - Abstract 3093: Clinical Factors Associated With Hypotension Within 12 Hours Of Antihypertensive Therapy In ED Stroke Patients. Adeoye, O; Hart, K.W.; Dahl, C.; Waymeyer, P.; Ewing, I.; Pancioli, A.; Lindsell, C. Univ of Cincinnati, Cincinnati, OH
Candidate Info
11
years in
workforce
5
years
at this job
BA
Communications
6

Clinical Research Coordinator

Served as Clinical Research Coordinator at Department of Psychiatry and Behavioral Neurobiology. Recruited subjects for research studies; administering questionnaires to determine eligibility, and conducted informed consent sessions. Worked with research professionals to assess neurocognitive/psychiatric status of potential patients, and review all medical, laboratory, and diagnostic data. Assisted patients by providing appropriate referrals to physicians, clinics, or agencies. Educated patients and patient representatives on the eligibility requirements, and application and insurance verification process to screen for applicable pediatric clinics.

  • Demonstrated the ability to interact with patients from diverse cultures and backgrounds.
  • Helped refine policies and procedures for Clinical Research Department in the areas of procedures, safety methods, aftercare planning and documentation.
  • Successfully learned and executed clinical trial protocols in accordance with state regulatory laws.
  • Recognized for superior performance and dedicated service committed through an award for "Outstanding Employee."
Candidate Info
12
years in
workforce
9
years
at this job
BS
Psychology
7

Research Coordinator

Detailed knowledge of GCP and ICH guidelines including basic understanding of regulatory documents.

  • Assessed Adverse Event (AE) and recorded Serious Adverse Event (SAE) in both paper and electronic data base and collected relevant documents in order to contact and follow up with the appropriate contact.
  • Obtained good understanding of the entire clinical trial process including informed consent obtained
  • Comprehensive knowledge of Clinical Research Alliance's S.O.P.'s for site management.
  • Prepared all study documents for Sponsor audit.
Candidate Info
6
years in
workforce
2
years
at this job
BA
Medicine
8

Clinical Research Coordinator Rn

Clinical research coordination of numerous Phase II and III studies in Diabetes, complicated Intra-Abdominal Infections, Influenza, Nutritional, Hepatitis C, Skin Infections, Thromboembolism and IBS.

  • Coordinated research activities in out-patient and in-patient hospital settings.
  • Provided in-service training to various hospital departments to ensure understanding of protocol specific study treatments and procedures.
  • Assisted in the informed consent process, screened potential patients for adult oncology clinical trials; assessed and monitored treatment patients for toxicities, dose modifications, and serious adverse events.
  • Provided patient/family/medical/nursing staff education related to clinical trials.
  • Assisted in accurate data collection/EDC entry, ordered all protocol requirements and obtained results; performed ECG's; phlebotomy/specimen collection; shipment of all required protocol specimens.
  • Attended Research meetings and trainings as needed and required.
Candidate Info
18
years in
workforce
4
months
at this job
BS
Nursing
MA
Public Health
9

Clinical Research Coordinator Ii

Ensured compliance with protocol guidelines and requirements of regulatory agencies; identified problems and/or inconsistencies and monitor patients' progress to include documentation and reporting of adverse events in the areas of neurology, sleep medicine, and pulmonology.

  • Facilitated regulatory management using FDA and USDA requirements. IRB reporting.
  • Conducted patient visits. Knowledge and utilization of Good Laboratory Practice (GLP), Good Clinical Practice (GCP), and Hazard Analysis Critical Control Points (HACCP).
  • Collected data, analyzed, and communicated the results of biological studies.
  • Developed forms, questionnaires and the application of research techniques; collaborate in writing of investigator-initiated protocols, and source documents for data collection.
  • Assisted investigator with protocol development and staff training on protocols and proper procedures.
Candidate Info
11
years in
workforce
2
years
at this job
BS
Nursing
MA
Master of Arts
10

Certified Clinical Research Coordinator

Accountable for overseeing all phases of clinical trials, assisted in budget preparation, and acted as liaison between physician and drug companies as well as IRB's.

  • Provided extensive in-service training for staff, physicians and ancillary personnel.
  • Supervised junior coordinators while working on my studies.
  • Controlled quality of data and reported research activities to team as a lead coordinator.
  • Facilitated completion of clinical charts and case report forms.
  • Wrote adverse event reports, obtained MD signatures, and submitted these to the sponsor and IRB.
  • Created source documents for data collection, which were incorporated and endorsed by pharmaceutical companies for use at other sites.
Candidate Info
11
years in
workforce
7
years
at this job
C
Certificate
C
Medical
C
Certificate

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