How do they match: Clinical Research Coordinators

  • Clinical Operations Specialist
  • Clinical Research Assistant
  • Clinical Research Specialist
  • Clinical Support Specialist
  • Clinical Trial Assistant
  • Clinical Trials Specialist

  • 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.

  • Instruct patients in the use of assistive equipment.