Senior Regulatory Affairs Lead – Oncology

Parabilis Medicines is seeking an Associate Director, Regulatory Affairs to lead regulatory strategy and execution across the product lifecycle in Cambridge, MA. This role focuses on advancing programs through optimized regulatory plans, with emphasis on NDA/BLA submissions and FDA interactions.

The position requires 7+ years in pharma/biotech, including at least 4 years in Regulatory Affairs, and strong cross-functional collaboration. Travel up to 10% is expected.