How do they match: Clinical Research Coordinators

  • Program Coordinator
  • Clinical Program Coordinator
  • Clinical Program Manager
  • Clinical Research Administrator

  • Confer with health care professionals to determine the best recruitment practices for studies.
  • Contact outside health care providers and communicate with subjects to obtain follow-up information.
  • Inform patients or caregivers about study aspects and outcomes to be expected.
  • Instruct research staff in scientific and procedural aspects of studies including standards of care, informed consent procedures, or documentation procedures.
  • 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 scientific literature, participate in continuing education activities, or attend conferences and seminars to maintain current knowledge of clinical studies affairs and issues.

  • Conduct employee training programs.
  • Promote products, services, or programs.