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Program Outcomes - Clinical Research Coordinator AAS

Learning Outcomes

Upon successful completion of the Clinical Research Coordinator AAS program, the learner will be able to:

  1. Compare/contrast the clinical research phases.
  2. Outline the process for data collection and documentation.
  3. Identify the elements of a clinical research protocol.
  4. Outline the study start-up process.
  5. Examine the regulatory aspects of the informed consent form and process.
  6. Perform a mock clinical trial.
  7. Manage medical records upholding privacy and security regulations.
  8. Identify professional research associations and review their respective associations with a research site.
  9. Complete Human Subject Training requirements.
  10. Categorize a Regulatory Binder and examine the essential documents required to adhere to regulatory compliance.
  11. Obtain Critical thinking skills necessary for a successful career as a CRC.
  12. Obtain professional skills necessary for a successful career as a CRC.
  13. Use computer programs commonly found in a research facility.
  14. Describe the structural organization of the body.
  15. Obtain specimens for diagnostic evaluation and testing.
  16. List the indications for use, dosage forms, generic and trade names for commonly used medications.
  17. Examine ethical considerations for research volunteers.
  18. Examine the regulations and guidelines for pharmaceutical, device, industry-sponsored and federally sponsored clinical trial design.
  19. Develop an on-site monitoring plan.
  20. Identify the regulatory agencies involved in clinical research.