Clinical Research Program Objectives

Upon completion of the BS in Clinical Research major, graduates will be able to:

1. Demonstrate a basic knowledge of scientific concepts related to research methodologies described in study protocols with emphasis on design and analysis of clinical trials, and regulatory compliance.
2. Apply aspects of human subject protection, ethical considerations and safety in the care and oversight of subjects participating in clinical trials.
3. Describe the process for development and regulation of drugs, devices, and biologicals.
4. Develop project management plans for the compliance, safety management, and handling of investigational products.
5. Conduct a comprehensive site(s) evaluation for compliance and operational requirements.
6. Design appropriate data management plans emphasizing varied data collection methods, security and quality control.
7. Demonstrate appropriate data collection methods to ensure participant anonymity and data integrity.
8. Critically appraise and synthesize existing literature for the development of research protocols, manuscripts and final reports.
9. Demonstrate competency in scientific writing and in preparation and delivery of oral presentations for research findings.
10. Implement principles and practice of leadership and professionalism in clinical research to interact effectively as an entry-level clinical research professional.