How do they match: Clinical Research Coordinators

  • Clinical Research Assistant
  • Clinical Trial Assistant

  • Identify protocol problems, inform investigators of problems, or assist in problem resolution efforts, such as protocol revisions.
  • Monitor study activities to ensure compliance with protocols and with all relevant local, federal, and state regulatory and institutional polices.
  • Register protocol patients with appropriate statistical centers as required.
  • Track enrollment status of subjects and document dropout information such as dropout causes and subject contact efforts.

  • Instruct patients in the use of assistive equipment.
  • Prepare operational progress or status reports.