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University of Utah PS Clinical Site Monitor in SALT LAKE CITY, Utah

Oversees, coordinates and conducts monitoring reviews of clinical trials and clinical research projects within the Department of Internal Medicine. Position provides independent regulatory oversight of all aspects of study conduct at the site, institutional, or network level. Ensures compliance with University policies, Food and Drug Administration (FDA) and Office of Human Research Protection (OHRP) regulations, Good Clinical Practice (GCP), and state and federal guidelines. Expertise in human subject research and experience working with the FDA and ICH GCP are required. Independently performs all on-site or remote monitoring activities.

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