How do they match: Clinical Research Coordinators

  • Instruct research staff in scientific and procedural aspects of studies including standards of care, informed consent procedures, or documentation procedures.
  • Dispense medical devices or drugs, and calculate dosages and provide instructions as necessary.
  • Prepare for or participate in quality assurance audits conducted by study sponsors, federal agencies, or specially designated review groups.

  • Instruct patients in the use of assistive equipment.