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| CLR 340 - Study and Site Management for Clinical Trials |
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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, principle investigator, sponsor, and contract research organization.
3.000 Credit hours 3.000 Lecture hours Levels: Undergraduate Schedule Types: Lecture School of Nursing Department Course Attributes: UnvStdy Critical Reasoning, UnvStdy Information Literacy Restrictions: Must be enrolled in one of the following Majors: Clinical Research Clinical Research May not be assigned one of the following Student Attributes: Online Accelerated Programs Prerequisites: Undergraduate level CLR 301 Minimum Grade of C |
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