How do they match: Clinical Research Coordinators

  • Plan, direct, or coordinate clinical research projects. Direct the activities of workers engaged in clinical research projects to ensure compliance with protocols and overall clinical objectives. May evaluate and analyze clinical data.

  • 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 proposed study protocols to evaluate factors such as sample collection processes, data management plans, or potential subject risks.

  • Plan facility layouts or designs.