Department: Clinical Research Coordinator
Program/Major Code: CRDCRP/CRP
CIP Code: 51.0719
Program Learning Outcomes
Upon successful completion of the program, the learner will be able to:
1. Explain the scientific concepts related to the design and analysis of clinical trials.
2. Apply the human subject protections and patient safety guidelines to the conduct of a clinical trial.
3. Identify how investigational products are developed and regulated.
4. Simulate study management and handling of investigational products’ best practices.
5. Examine the strategies to manage participant recruitment, retention, compliance, and track study activities.
6. Develop a process for a data quality assurance life-cycle (development, collection, analysis).
7. Model the principles of leadership and professionalism in clinical research.
8. Justify the teamwork skills necessary for conducting a clinical trial.
Semester Pathway
This pathway is a suggested sequence of courses for your program of study. Work with an advisor to develop a unique pathway for you based on your placement recommendations, any prior college courses, and your specific situation.
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