How do they match: Clinical Research Coordinators

  • Instruct research staff in scientific and procedural aspects of studies including standards of care, informed consent procedures, or documentation procedures.
  • Oversee subject enrollment to ensure that informed consent is properly obtained and documented.
  • Prepare study-related documentation, such as protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, or progress reports.
  • Track enrollment status of subjects and document dropout information such as dropout causes and subject contact efforts.

  • Maintain regulatory or compliance documentation.