How do they match: Clinical Research Coordinators

  • Clinical Operations Specialist
  • Clinical Research Specialist
  • Clinical Support Specialist
  • Clinical Trials Specialist

  • Code, evaluate, or interpret collected study data.
  • Contact industry representatives to ensure equipment and software specifications necessary for successful study completion.
  • Direct the requisition, collection, labeling, storage, or shipment of specimens.
  • Participate in the development of study protocols including guidelines for administration or data collection procedures.
  • Perform specific protocol procedures such as interviewing subjects, taking vital signs, and performing electrocardiograms.
  • Prepare for or participate in quality assurance audits conducted by study sponsors, federal agencies, or specially designated review groups.
  • Review proposed study protocols to evaluate factors such as sample collection processes, data management plans, or potential subject risks.

  • Interview employees, customers, or others to collect information.