How do they match: Clinical Research Coordinators

  • Monitor study activities to ensure compliance with protocols and with all relevant local, federal, and state regulatory and institutional polices.
  • Prepare for or participate in quality assurance audits conducted by study sponsors, federal agencies, or specially designated review groups.
  • Record adverse event and side effect data and confer with investigators regarding the reporting of events to oversight agencies.
  • Register protocol patients with appropriate statistical centers as required.
  • Track enrollment status of subjects and document dropout information such as dropout causes and subject contact efforts.

  • Communicate with government agencies.
  • Prepare operational progress or status reports.