ARTBIO seeks a Senior Director, Regulatory Affairs to lead regulatory interactions and submissions across clinical-stage radiopharmaceutical programs. You will coordinate medical writing and translate R&D data into compliant regulatory communications, guiding high-quality INDs, amendments, annual reports, and lifecycle submissions. You will partner with Clinical, Medical, CMC, Quality, and other functions to maintain submission narratives, regulatory plans, trackers, and archives, ensuring

Also on the board Same function, level within a rung

Level

Manager

Location

Somerville, MA

Occupation

Regulatory Affairs Managers

Industry

Electromedical and Electrotherapeutic Apparatus Manufacturing

Posted

today

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