Senior Director, CMC Regulatory Affairs — Hybrid (San Diego)

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.