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.

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

  • Plan facility layouts or designs.
  • Conduct financial or regulatory audits.
  • Maintain regulatory or compliance documentation.
  • Monitor organizational compliance with regulations.