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VP, Regulatory Affairs: Global Approvals Leader

Akebia Therapeutics ®, Inc., Cambridge, Massachusetts, us, 02140

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A biotechnology company in Cambridge is seeking a VP of Regulatory Affairs to lead the strategy for product approvals and compliance. This role involves overseeing regulatory submissions, managing a team, and fostering relationships with regulatory bodies like the FDA. The ideal candidate has over 10 years of experience in drug development and regulatory affairs, with proven leadership skills and a strong understanding of FDA and EMA regulations. A competitive salary and comprehensive benefits package is offered. #J-18808-Ljbffr