Clinical Research Coordinator Resume Sample

Clinical Research Coordinators work in a clinical research environment to ensure the smooth running of clinical trials. They set up protocols, maintain confidentiality and monitor patient safety during trials, communicate with patients and monitor their progress, coordinate lab activities, and train new research assistants. Top skills in this position include project management, report writing, data analysis, clinical research knowledge, and human subject protection. A bachelor’s degree is required for this position, but previous experience working in the clinical research field is preferred.

The Best Clinical Research Coordinator Resume Samples

These are some examples of accomplishments we have handpicked from real Clinical Research Coordinator resumes for your reference.

Clinical Research Coordinator

  • 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.

Clinical Research Coordinator

  • 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.

Clinical Research Coordinator

  • 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.

Clinical Research Coordinator

  • 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.

Clinical Research Coordinator

  • 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.

Clinical Research Coordinator

  • 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.

Clinical Research Coordinator

  • 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.

Clinical Research Coordinator

  • 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.

Clinical Research Coordinator

  • 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.

Clinical Research Coordinator

  • 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.

Clinical Research Coordinator

  • Multi-modal study integrating psychosocial, neuropsychological, neuroimaging, and genomics research to identify predictive biomarkers in prodromal/preonset psychosis.
  • Conducted semi-structured and structured clinical interviews and computerized neurocognitive battery (CNB) with research participants.
  • Wrote and prepared summaries of impressions to be presented at case conference where prodromal status is determined by consensus.

Clinical Research Coordinator

  • Assessed clinical performance and ergonomics of devices; provided feedback to multidisciplinary R&D team.
  • Maintained detailed logs regarding history of subject participation, employee trainings, device components, etc.
  • Assisted in the development of fail-safe features for new device mechanisms to ensure subject safety.
  • Designed procedures for device validation testing including optical, mechanical, electrical, and software.

Wrap Up

Resumes are a crucial aspect of any job search. In order to make a good first impression, it is important that your resume be formatted and written professionally.

Hope these samples gave you an idea of what your resume should look like and some tips on how to make sure that your resume stands out from the rest.

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