CMC Regulatory Strategy Lead, Oncology

A biotechnology company is seeking an Associate Director of Regulatory Affairs CMC to develop and execute CMC regulatory strategies for its product pipeline. Responsibilities include providing CMC expertise for drug development, ensuring compliance with quality systems, and collaborating with internal teams. Candidates should have a minimum of 8 years in clinical research or biotech and possess strong strategic and communication skills. The role is based in Boston, MA with a competitive compensation package.
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