Senior Regulatory Affairs Manager: Global Clinical Trials
Xerispharma
Xeris Pharmaceuticals, Inc. in Chicago is seeking a Manager of Regulatory Affairs to lead regulatory submissions for global clinical programs. You will steer INDs, CTAs, amendments, and annual reports, while shaping regulatory strategy and ensuring compliance across phases. You will collaborate with Clinical Operations, Medical Writing, and other functions to assemble robust submissions, monitor timelines, and support health authority interactions as needed. #J-18808-Ljbffr Xerispharma
Vacancy posted 15 hours ago
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