Senior Vice President, Head of Global Regulatory Affairs

This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Senior Vice President, Head of Global Regulatory Affairs based in United States.
This is a senior executive role responsible for shaping and executing global regulatory strategy across the full drug development lifecycle.
You will lead regulatory strategy spanning CMC, preclinical, clinical development, commercialization, and post-approval activities across multiple regions.
The role serves as a key advisor to senior leadership, providing guidance on regulatory risk, development strategy, launch timing, and lifecycle management.
You will lead a regulatory organization while partnering closely with clinical, commercial, medical, legal, quality, safety, supply chain, and market access teams.
The position combines strategic leadership with hands-on oversight of submissions, health authority interactions, regulatory operations, and compliance.
You will help prepare products for late-stage development, global registration, launch, and ongoing commercialization.
This is a remote U.S.-based position with travel as needed to support business and regulatory requirements.

Employment type
Full-time

Work arrangement
Yes