Director or Senior Director, Regulatory Affairs
Kymera Therapeutics
Location: Watertown, MA, United States
Senior Manager, Regulatory Affairs at Kymera Therapeutics in Watertown, MA **What you'll do** - Lead regulatory activities across drug development programs. - Compile and author regulatory submission packages. - Provide oversight for CRO regulatory groups. - Support health authority interactions and submissions. **What they're looking for** - Experience in regulatory affairs in biotech. - Strong understanding of regulatory submission processes. - Ability to work cross-functionally in a dynamic environment. - Excellent communication and leadership skills. **Details** - Location: Watertown, MA - Type: Not specified
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