How do they match: Clinical Research Coordinators

  • Communicate with laboratories or investigators regarding laboratory findings.
  • Monitor study activities to ensure compliance with protocols and with all relevant local, federal, and state regulatory and institutional polices.
  • 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.

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