Associate Director, Regulatory Submission Project Management
Regeneron Pharmaceuticals • Tarrytown, NY • Posted June 29, 2026
About the Role
**Build our future together:**
At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an **Associate Director** to join our **Regulatory Affairs** team. This individual will be responsible for providing senior leadership in the strategic planning and execution of regulatory milestones from IND Project Approval (IPA) through post marketing. They will serve as the Reg PM lead for assigned therapeutic area(s) (TA) and drives organizational excellence and consistency across regulatory programs within the function.
**When & where:**
+ Work Location: Tarrytown, NY or Warren, NJ
+ Hybrid; 4 days per week on site
**Discover your role:**
+ Demonstrates independent and strategic thinking, serves as a subject matter expert, and provides leadership and direction to the Reg PM team. Acts as a key decision-maker and escalation point, partnering closely with senior management t...
At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an **Associate Director** to join our **Regulatory Affairs** team. This individual will be responsible for providing senior leadership in the strategic planning and execution of regulatory milestones from IND Project Approval (IPA) through post marketing. They will serve as the Reg PM lead for assigned therapeutic area(s) (TA) and drives organizational excellence and consistency across regulatory programs within the function.
**When & where:**
+ Work Location: Tarrytown, NY or Warren, NJ
+ Hybrid; 4 days per week on site
**Discover your role:**
+ Demonstrates independent and strategic thinking, serves as a subject matter expert, and provides leadership and direction to the Reg PM team. Acts as a key decision-maker and escalation point, partnering closely with senior management t...