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Global CMC Regulatory Affairs Lead

Olema Oncology, San Francisco

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A biotechnology company in San Francisco is seeking an Associate Director, Regulatory Affairs CMC. You will lead the development and execution of CMC regulatory strategies for product(s) in development and post-approval. The ideal candidate should have 8+ years in clinical research with at least 6 years in Regulatory Affairs. Strong expertise in CMC regulations and excellent communication skills are essential. The position requires a bachelor's degree in a scientific field and may involve some travel.
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