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.
  • Communicate with laboratories or investigators regarding laboratory findings.
  • Contact industry representatives to ensure equipment and software specifications necessary for successful study completion.
  • Identify protocol problems, inform investigators of problems, or assist in problem resolution efforts, such as protocol revisions.
  • 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.
  • Record adverse event and side effect data and confer with investigators regarding the reporting of events to oversight agencies.

  • Communicate with government agencies.