How do they match: Clinical Research Coordinators

  • Collaborate with investigators to prepare presentations or reports of clinical study procedures, results, and conclusions.
  • Contact industry representatives to ensure equipment and software specifications necessary for successful study completion.
  • Develop advertising and other informational materials to be used in subject recruitment.
  • 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.
  • Review scientific literature, participate in continuing education activities, or attend conferences and seminars to maintain current knowledge of clinical studies affairs and issues.

  • Develop promotional materials.
  • Prepare operational progress or status reports.
  • Purchase materials, equipment, or other resources.