Senior Director, CMC Regulatory Affairs — Hybrid (San Diego)
Protego Bio
Protego Biopharma is seeking a Senior Director, Regulatory Affairs (CMC) to lead the global CMC regulatory strategy for a first-in-class small molecule program advancing toward NDA/MAA submission. The role combines strategy, authoring, and hands-on submissions, reporting to the SVP of Regulatory Affairs. Responsibilities include global CMC strategy, health authority engagement, and cross-functional collaboration with QA, Analytical Development, Clinical, and Program Management. #J-18808-Ljbffr Protego Bio
Vacancy posted 4 days ago
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