Oncology Regulatory Affairs Strategy Manager – Hybrid

Regeneron Pharmaceuticals, Inc. in the United States seeks a Manager to join the Regulatory Affairs Strategy Oncology team.

You will coordinate preparation, submission, and maintenance of global regulatory submissions and assist in agency meetings and briefing documents. This role requires an MD, PhD, or PharmD with 2+ years of regulatory experience, experience with US FDA and international guidelines, and strong written and verbal communication.

Consider building your career as a Oncology Regulatory Affairs Strategy Manager – Hybrid at Regeneron Pharmaceuticals, Inc (USA).

The following role is for a Oncology Regulatory Affairs Strategy Manager – Hybrid with Regeneron Pharmaceuticals, Inc (USA).

Our group is growing, and we are hiring a Oncology Regulatory Affairs Strategy Manager – Hybrid in KY, United States.

This role is for the Oncology Regulatory Affairs Strategy Manager – Hybrid role at Regeneron Pharmaceuticals, Inc (USA).