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Program Outcomes - Clinical Research Coordinator Certificate

Learning Outcomes

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

  1. Compare/contrast the clinical research phases.
  2. Outline the process for data collection and documentation.
  3. Outline the study start-up process.
  4. Perform a mock clinical trial.
  5. Manage medical records upholding privacy and security regulations.
  6. Identify the regulatory agencies involved in clinical research.
  7. Complete human subject training requirements.
  8. Categorize a regulatory binder and examine essential documents required to adhere to regulatory compliance.
  9. Obtain critical thinking skills necessary for a successful career as a CRC.
  10. Obtain professional skills necessary for a successful career as a CRC.
  11. Use computer programs commonly found in a research facility.
  12. Describe the structural organization of the body.
  13. Obtain specimens for diagnostic evaluation and testing.
  14. List the indications for use, dosage forms, generic and trade names for commonly used medications.