How do they match: Clinical Research Coordinators

  • Confer with health care professionals to determine the best recruitment practices for studies.
  • 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.
  • Solicit industry-sponsored trials through contacts and professional organizations.

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