How do they match: Clinical Research Coordinators

  • Code, evaluate, or interpret collected study data.
  • 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.
  • Review proposed study protocols to evaluate factors such as sample collection processes, data management plans, or potential subject risks.
  • Review scientific literature, participate in continuing education activities, or attend conferences and seminars to maintain current knowledge of clinical studies affairs and issues.

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