Clinical Research Coordinator Resume Samples

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Clinical Research Coordinators manage clinical trials and assess a drug's or medical device benefits and risks. Some usual work duties listed on a Clinical Research Coordinator resume are handling daily activities, interviewing and hiring staff, implementing policies, writing reports, budgeting, and organizing meetings. Qualifications such as healthcare management, financial skills, leadership, analytical thinking and accuracy are often seen on the most successful resume samples. A Bachelor's Degree in a relevant field is required. Ethics and case management expertise are crucial too.

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1

Clinical Research Coordinator

Coordinated schedules of patients, therapists and doctors while adhering to strict protocol
guidelines.

  • Executed and supervised 12 clinical research studies at a time, from recruitment of subjects to end of study.
  • Recruited 6-8 patients for each clinical trial, exceeding the enrollment goals.
  • Designed source documents for each clinical research study thereby optimizing the amount of correct data captured at each patient visit.
  • Secured business relationships with advertising vendors and worked with them to utilize
  • Advised Principal Investigator on decisions such as trial acquisition, advertising and patient interactions.
Candidate Info
3
years in
workforce
2
years
at this job
BA
Psychology
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

Clinical Research Coordinator

Assisted Medical Oncologists, Surgeons, and Nurse Case Managers in assessing patient eligibility

  • Effectively met deadlines and consistently exceeded expectation for timely data collection and submission
  • Evaluated needs of patients newly diagnosed with breast cancer and brain cancer to best serve as their advocate
  • Oversaw adherence to study protocol for radiographic and clinical patient evaluations, treatment administration, and collection, processing, and shipping of biological specimens
  • Maintained accurate records of Adverse Events, expedited reports of Serious Adverse Events, and conducted neurocognitive assessments and mental status exams throughout a patient's treatment
  • Collaborated with Pharmacists and Medical Oncologists to build and manage patient treatment plans
  • Ensured accurate billing of study versus standard of care procedures and corrected charges when necessary
Candidate Info
14
years in
workforce
1
year
at this job
BA
Cognitive Science
4

Clinical Research Coordinator II

Responsible for coordination of clinical research activities conducted within the Joint Penn-CHOP Center for Digestive, Liver and Pancreatic Medicine, whose mission is to help adolescents take the step from Pediatric care to Adult care, conducting research in the Center for Pediatric Inflammatory Bowel Disease.

  • Coordinated, organized and maintained all study documentation including source documentation, case report forms, study and regulatory binders and patient binders.
  • Screened subjects from the daily clinic schedule and confirm eligibility of potential study subjects.
  • Recruited approximately 300 subjects for various studies and administered informed consent.
  • Scheduled study visits and necessary testing including procuring blood, urine, serum, and intestinal specimens.
  • Prepared and processed all documentation through the Institutional Review Board (IRB), including submissions, continuing reviews, amendments and adverse event reporting.
  • Prepared for and participated in audits conducted by sponsors and other oversight entities such as CHOP's Regulatory and Compliance Office.
Candidate Info
31
years in
workforce
6
years
at this job
BA
Business Administration
5

Clinical Research Coordinator

Worked with and under the Principal Investigator; supported, facilitated, and coordinated the daily clinical trial activities. Independently handled large caseloads (30-50) of patients, collected data as required by protocols.

ACHIEVEMENTS:

  • Maintained effective/ongoing communication with research participants/sponsors increasing customer satisfaction
  • Coordinated appropriate and timely payments to participants ensuring sustained enrollments
  • Implemented approved recommendations for audit findings reducing repeat discrepancies
  • Great problem-solving, and analytical skills were possessed to maintain job with ease
Candidate Info
10
years in
workforce
2
years
at this job
Nursing Credentials
6

Clinical Research Coordinator

Maintained IRB annual renewals and refined research protocols; acted as a liaison with physician and drug companies

  • Prepare and participate in conducting patient and study visits
  • Managed regulatory documents and clinical trial manuals; designed patient tracking charts using spreadsheets and formulated source documents and data collection charts
  • Facilitated completion of clinical charts and case report forms. Controlled quality of data retrieved from patient records and reported research activities to team.
  • Knowledge of ICH and local regulatory authority regulations regarding drug research and development
Candidate Info
16
years in
workforce
5
years
at this job
BS
Microbiology
7

Certified Clinical Research Coordinator

Operated as a certified clinical research coordinator under the direction of the principal investigator in a private urology practice involved in phase 1 through phase 4 pharmaceutical studies, including prostate cancer, over active bladder, incontinence, SPV virus, sperm testing, sexual dysfunctions

  • Coordinated all phases of clinical trials study start up to study closure; acted as liaison between the physician and sponsor
  • Managed regulatory documents and clinical trials manuals; designed patient tracking charts using spreadsheets and formulated source documents and data collection charts
  • Facilitated the completion of clinical charts and case report forms
  • Controlled quality of data retrieved from hospital records and reported research activities to team
  • Wrote severe adverse event reports and obtained MD signatures; submitted to sponsor and the IRB
  • Implemented recruitment strategies to get PI's more involved with subject enrollment
  • Identified problems and/ or inconsistencies and monitor patients' progress to include documentation and reporting of adverse events
Candidate Info
1
year in
workforce
1
year
at this job
C
Certificate
C
Clinical Research Coordinator Basic Training
C
Business Skills Training
8

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
9

Clinical Research Coordinator

US Oncology research network

  • Clinical coordination of numerous Phase II and Phase III studies for solid and hematologic diseases.
  • Demonstrated ability, efficiency and flexibility in working at 5 different clinic sites as needed to meet research department and staffing needs.
  • Responsible for assisting in the informed consent process, screening potential patients for adult oncology clinical trials; assessed treatment patients for toxicities, dose modifications, and serious adverse events.
  • Provided patient/family/medical/nursing staff education related to clinical trials; assisted physicians in tumor assessments of subjects as per protocol.
  • Assisted in accurate data collection, ordered all protocol requirements and obtained results; performed ECG's; prepared, handled and shipped all required research specimens.
  • Attended research/clinic meetings and trainings bi-monthly or more as needed and required.
Candidate Info
15
years in
workforce
2
years
at this job
BS
Nursing
MA
Public Health
10

Clinical Research Coordinator

Acted as project manager for 3 clinical trials simultaneously.

  • Managed all day-to-day activities necessary to facilitate the successful completion of each trial.
  • Developed and executed plan to ensure that all aspects of each study were completed with strict adherence to protocol.
  • Trained 9 clinic personnel to effectively complete study specific procedures and documentation.
  • Evaluated and analyzed clinical research data to ensure accuracy and consistency between source documents as well as proper, timely reporting of critical study events.
  • Assisted in preparation for United States Food and Drug Administration and Institutional Review Board audits.
  • Responsible for identifying 3 clinical protocols and implementing them as project lead.
  • Designed and implemented recruitment strategies that earned company the title of highest national subject enrollment with 150 subjects for a HIV clinical trial.
Candidate Info
4
years in
workforce
2
years
at this job
BA
Psychology

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