Global Regulatory Strategy Lead - Clinical Trials & Submissions

Spyre Therapeutics, Inc. in the United States is seeking a senior Regulatory Affairs professional to manage global regulatory activities for their IBD program, shaping strategies to enable clinical trials and marketing applications.

You will lead preparation and submission of regulatory applications to the FDA, EMA, and other health authorities, ensuring timely approvals while coordinating with research, clinical, and technical teams.

As a Global Regulatory Strategy Lead
- Clinical Trials & Submissions, you will play an important part at Spyre Therapeutics, Inc. in United States.

This Full Time position is for the Global Regulatory Strategy Lead
- Clinical Trials & Submissions role at Spyre Therapeutics, Inc.

We are seeking a motivated Global Regulatory Strategy Lead
- Clinical Trials & Submissions to join Spyre Therapeutics, Inc. in United States.

Consider building your career as a Global Regulatory Strategy Lead
- Clinical Trials & Submissions at Spyre Therapeutics, Inc.