CRC255 — Study and Site Coordination
3 , 3 lecture periods 0 lab periods Foundational research & regulatory concepts. Includes an introduction to strategies for implementing a clinical trial and managing site operations to ensure data integrity and participant safety. Also includes professional and ethical practices, site feasibility, participant recruitment and retention, and site-specific procedures. Includes practical experience through Good Documentation Practices, data collection, product accountability, and informed consent best practices. Course Learning
Prerequisites: CRC151