How do they match: Clinical Research Coordinators

  • 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.
  • Participate in preparation and management of research budgets and monetary disbursements.
  • Review scientific literature, participate in continuing education activities, or attend conferences and seminars to maintain current knowledge of clinical studies affairs and issues.

  • Prepare medications or medical solutions.
  • Prepare operational progress or status reports.