How do they match: Clinical Research Coordinators

  • Prepare for or participate in quality assurance audits conducted by study sponsors, federal agencies, or specially designated review groups.
  • Prepare study-related documentation, such as protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, or progress reports.
  • Arrange for research study sites and determine staff or equipment availability.
  • Assess eligibility of potential subjects through methods such as screening interviews, reviews of medical records, or discussions with physicians and nurses.
  • Collaborate with investigators to prepare presentations or reports of clinical study procedures, results, and conclusions.
  • Contact industry representatives to ensure equipment and software specifications necessary for successful study completion.
  • Dispense medical devices or drugs, and calculate dosages and provide instructions as necessary.
  • Organize space for study equipment and supplies.
  • Participate in preparation and management of research budgets and monetary disbursements.

  • Prepare medications or medical solutions.
  • Prepare operational progress or status reports.
  • Calculate numerical data for medical activities.
  • Instruct patients in the use of assistive equipment.
  • Perform clerical work in medical settings.
  • Purchase materials, equipment, or other resources.