How do they match: Clinical Research Coordinators

  • Register protocol patients with appropriate statistical centers as required.
  • Maintain required records of study activity including case report forms, drug dispensation records, or regulatory forms.
  • Monitor study activities to ensure compliance with protocols and with all relevant local, federal, and state regulatory and institutional polices.

  • Conduct financial or regulatory audits.
  • Maintain regulatory or compliance documentation.
  • Monitor organizational compliance with regulations.