How do they match: Clinical Research Coordinators

  • Clinical Research Assistant
  • Clinical Trial Assistant

  • Register protocol patients with appropriate statistical centers as required.
  • Identify protocol problems, inform investigators of problems, or assist in problem resolution efforts, such as protocol revisions.
  • Maintain required records of study activity including case report forms, drug dispensation records, or regulatory forms.
  • Monitor study activities to ensure compliance with protocols and with all relevant local, federal, and state regulatory and institutional polices.

  • Conduct financial or regulatory audits.
  • Instruct patients in the use of assistive equipment.
  • Maintain regulatory or compliance documentation.
  • Monitor organizational compliance with regulations.