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.
  • Developed and implemented research protocols, with the assistance of licensed pharmacists, designed to test over 25 medications in relation to their effectiveness on the elderly.
  • Effectively tracked and analyzed data on drug activity, side effects, as well as adverse reactions observed at clinical trial stages.

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 and execution of programs that contributed to a 32% growth of the trial within 1 fiscal year.
  • Served as a Clerical Assistant to the Clinical Research Coordinator who designed over twenty different clinical trials by utilizing internal databases, information technicians, and clinical pharmacists.
  • Researched patient demographics for the study to ensure appropriate matching of characteristics within sub-population groups.

Clinical Research Coordinator

  • Effectively met deadlines and consistently exceeded expectations 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 various agencies in order that all data matched within preset criteria for each clinical trial.

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.
  • Evaluated, recommended, and documented selection of patients for participation in clinical trial protocols; identified and dispensed medications by 11 physicians.

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.
  • Coordinated research protocols to meet the goals of specific projects including recruiting patients to receive experimental or approved treatments under IRB regulations.
  • Supervised team members to ensure proper handling of sensitive information; created a positive work environment by resolving conflicts; maintained efficient interaction with other departments.

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 the team.
  • Knowledge of ICH and local regulatory authority regulations regarding drug research and development.
  • Assisted in the development of study methodology by collaborating with investigators, medical and laboratory staff, and other clinical research coordinators.

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 the team.
  • Diagnosed and treated patients in a timely manner; guaranteed patient satisfaction even with more complex conditions.

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 the writing of investigator-initiated protocols, and source documents for data collection.
  • Saved two family members from potential death by monitoring vital signs and administering first aid.

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.
  • Participated in the study with oversight from Clinical Managers regarding the collection of data from patients on a daily basis over an entire year.
  • Obtained enough experience in evaluation, treatment, and implementation of clinical research procedures to join the team as a clinical research coordinator.

Clinical Research Coordinator

  • Managed all day-to-day activities necessary to facilitate the successful completion of each trial.
  • Developed and executed a 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.
  • Received outstanding quality award for excellent performance; followed up on every prescription to ensure each patient was satisfied with their care, which usually culminated in a compliment or recommendation by the primary medical professional involved.

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 conferences where prodromal status is determined by consensus.
  • Coordinated the study to be conducted through the group’s Clinical Research Department; reviewed and researched all vials, medications, and equipment; edited questionnaires and spreadsheets; entered data in the computer.
  • Reviewed, selected, and amended “protocols” for various tests.

Clinical Research Coordinator

  • Assessed clinical performance and ergonomics of devices; provided feedback to the multidisciplinary R&D team.
  • Maintained detailed logs regarding the history of subject participation, employee training, 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.
  • Revised protocols by changing dosing time spans or increasing dosages of certain medications when necessary.

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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