Hybrid Senior Manager, Regulatory Affairs - Oncology

Medella Life is seeking a Senior Manager of Regulatory Affairs to develop strategies for oncology programs in a clinical-stage biotech setting. Responsibilities include leading regulatory submissions, partnering with cross-functional teams, and ensuring compliance with FDA regulations. Candidates should have a Bachelor’s degree and over seven years of experience in Regulatory Affairs, specifically in the biotech industry. The role offers a competitive compensation package with a hybrid work schedule requiring 2-3 days on-site in Massachusetts.
This position is for the Hybrid Senior Manager, Regulatory Affairs - Oncology role at Medella Life. Please review the full job details above before applying. If your experience matches this role, we encourage you to apply. All applications are reviewed carefully by our team. The position is based in MA, United States.