How do they match: Clinical Research Coordinators

  • Collaborate with investigators to prepare presentations or reports of clinical study procedures, results, and conclusions.
  • Maintain required records of study activity including case report forms, drug dispensation records, or regulatory forms.
  • Prepare study-related documentation, such as protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, or progress reports.
  • Record adverse event and side effect data and confer with investigators regarding the reporting of events to oversight agencies.

  • Prepare operational progress or status reports.