Director, Regulatory Affairs
Lead and execute the regulatory strategy for CAR T programs, serving as the primary regulatory representative, guiding activities across preclinical, clinical, and manufacturing stages, partnering with internal teams and external partners. Work cross-functionally with Clinical, CMC, Quality, and Patient Operations to plan and manage regulatory submissions, including INDs, IND amendments, and meeting packages. The ideal candidate brings experience in Regulatory Affairs within a clinical-stage biotech.
$195,000–$210,000
/yr