How do they match: Clinical Research Coordinators

  • Dispense medical devices or drugs, and calculate dosages and provide instructions as necessary.
  • Maintain required records of study activity including case report forms, drug dispensation records, or regulatory forms.
  • Order drugs or devices necessary for study completion.
  • Prepare for or participate in quality assurance audits conducted by study sponsors, federal agencies, or specially designated review groups.
  • Record adverse event and side effect data and confer with investigators regarding the reporting of events to oversight agencies.

  • Communicate with government agencies.