How do they match: Clinical Research Coordinators

  • Code, evaluate, or interpret collected study data.
  • Direct the requisition, collection, labeling, storage, or shipment of specimens.
  • Monitor study activities to ensure compliance with protocols and with all relevant local, federal, and state regulatory and institutional polices.
  • Participate in the development of study protocols including guidelines for administration or data collection procedures.
  • Register protocol patients with appropriate statistical centers as required.
  • Review proposed study protocols to evaluate factors such as sample collection processes, data management plans, or potential subject risks.
  • Track enrollment status of subjects and document dropout information such as dropout causes and subject contact efforts.

  • Interview employees, customers, or others to collect information.
  • Prepare operational progress or status reports.