Clinical Research Coordinator Resume Sample

These are some examples of job descriptions 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.

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