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Job description
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.
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Worksite address
san diego, CA, 92189, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.