Kymera Therapeutics is seeking a senior Regulatory Affairs CMC leader to drive global CMC strategies for degrader programs from early development through NDA/MAA submissions. You will collaborate with CMC, Quality, and Clinical teams to align regulatory plans with program timelines and ensure readiness for health authority interactions. The role emphasizes hands-on CMC submissions experience for small molecule programs, lifecycle management, and cross-functional leadership in a fast-paced

Also on the board Same function, level within a rung

Level

Manager

Location

Oklahoma City, OK

Occupation

Regulatory Affairs Managers

Industry

Research and Development in Biotechnology (except Nanobiotechnology)

Posted

yesterday

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