How do they match: Clinical Research Coordinators

  • Track enrollment status of subjects and document dropout information such as dropout causes and subject contact efforts.
  • Maintain contact with sponsors to schedule and coordinate site visits or to answer questions about issues such as incomplete data.
  • 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.

  • Maintain knowledge of current developments in area of expertise.
  • Maintain operational records.
  • Maintain regulatory or compliance documentation.