CLR 340 - Study and Site Management for Clinical Trials

Operational aspects of clinical trials at the site level, including financial, personnel, and legal considerations. Introduces relevant regulations and guidelines including ICH GCP. Includes discussion of roles, responsibilities, and perspectives of the subject, clinical study coordinator, prinicipal investigator, sponsor, and contract research organization.

Credit Hours: 3

Prerequisite Courses: CLR 301 with a C or better.
Additional Restrictions/Requirements: Only open to students within the Clinical Research major.
University Studies: Building Competencies/Information Literacy
Course Repeatability: Course may not be repeated. Maximum Repeatable Hours: 3

Click here for the Fall 2024 Class Schedule.