CLR 340 - Study and Site Management for Clinical Trials Credits: 3
Corequisite: CLR 301 . Only open to students within the Clinical Research major. 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. Partially satisfies University Studies IV: Building Competencies/Information Literacy.
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