How do they match: Clinical Research Coordinators

  • Program Coordinator
  • Clinical Program Coordinator
  • Clinical Program Manager

  • Instruct research staff in scientific and procedural aspects of studies including standards of care, informed consent procedures, or documentation procedures.
  • Maintain required records of study activity including case report forms, drug dispensation records, or regulatory forms.
  • 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.