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In collaboration with investigators, responsible for tracking and completing protocol feasibility questionnaires. Coordinates Critical Document Collection to facilitate the timely opening of trials at the site. Communicates and collaborates with central operations and data management to identify and resolve any regulatory issues. Maintains Protocol Regulatory Documents in
Posted 1 day ago
PMI (Project Management Institute)
- Anchorage, AK / Birmingham, AL / Little Rock, AR / 47 more...
Government Relations Manager United States Virtual Req #463 Thursday, December 28, 2023 Want to help people learn the newest ways of working and getting things done? How you'll make a difference You will be responsible for planning, developing and executing a strong positive government relations and advocacy program for PMI. You will be fostering a community relationship
Posted 10 days ago
The Regulatory Affairs Coordinator is responsible for providing central management and regulatory oversight for clinical trials and investigator initiated studies for The Division of Gastroenterology and Hepatology. This position will work closely with Principal Investigators, Research Development Manager, the department's administration team, and other departments and ce
Posted Today
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