How do they match: Clinical Research Coordinators

  • Contact industry representatives to ensure equipment and software specifications necessary for successful study completion.
  • Instruct research staff in scientific and procedural aspects of studies including standards of care, informed consent procedures, or documentation procedures.
  • Review scientific literature, participate in continuing education activities, or attend conferences and seminars to maintain current knowledge of clinical studies affairs and issues.

  • Advise customers on technical or procedural issues.
  • Promote products, services, or programs.