This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Senior Director, Global Regulatory Affairs – Biotech Unit based in United States.

This is a senior individual contributor role shaping global regulatory strategy for innovative oncology development programs and external biotech partnerships.
You will provide strategic and operational regulatory leadership across assets from early development through approval and lifecycle management.
The role spans major global markets, including the US, China, and Europe, and requires deep expertise in FDA and international regulatory frameworks.
You’ll work at the intersection of regulatory strategy, clinical development, scientific innovation, and business priorities.
As a key advisor to cross-functional and partnership teams, you’ll help resolve complex regulatory challenges and accelerate development timelines.
The environment is highly collaborative, global, and entrepreneurial, with significant opportunity to influence new partnership models and development approaches.
This position offers the chance to contribute directly to programs designed to expand access to impactful oncology treatments worldwide.

What the job really is