How do they match: Clinical Research Coordinators

  • Clinical Operations Specialist
  • Clinical Research Specialist
  • Clinical Support Specialist
  • Clinical Trials Specialist

  • Collaborate with investigators to prepare presentations or reports of clinical study procedures, results, and conclusions.
  • Contact industry representatives to ensure equipment and software specifications necessary for successful study completion.
  • Instruct research staff in scientific and procedural aspects of studies including standards of care, informed consent procedures, or documentation procedures.
  • Participate in the development of study protocols including guidelines for administration or data collection procedures.
  • Perform specific protocol procedures such as interviewing subjects, taking vital signs, and performing electrocardiograms.
  • Prepare for or participate in quality assurance audits conducted by study sponsors, federal agencies, or specially designated review groups.
  • Prepare study-related documentation, such as protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, or progress reports.
  • Schedule subjects for appointments, procedures, or inpatient stays as required by study protocols.

  • Advise customers on technical or procedural issues.
  • Develop organizational methods or procedures.