How do they match: Clinical Research Coordinators

  • Clinical Research Assistant
  • Clinical Trial Assistant

  • 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.
  • Collaborate with investigators to prepare presentations or reports of clinical study procedures, results, and conclusions.
  • Identify protocol problems, inform investigators of problems, or assist in problem resolution efforts, such as protocol revisions.
  • Participate in preparation and management of research budgets and monetary disbursements.

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