Senior Medical Director, Clinical Development, CV/Renal/Metabolism

Regeneron Pharmaceuticals • Warren, MA

10d

About The Position

Regeneron is seeking a Senior Medical Director, Clinical Development to join its Cardiovascular/Renal/Metabolism team, supporting programs focused on obesity and related comorbidities. The role serves as Scientific and Medical Lead for clinical teams, guiding development strategy and regulatory submissions in collaboration with Operational Leads, discovery teams, and Global Patient Safety. It reports to an Executive Medical Director, Internal Medicine.

The position is based in Tarrytown, New York; Cambridge, Massachusetts; or Warren, New Jersey, and includes 10% travel to relevant conferences. Regeneron describes its total rewards package as potentially including annual bonuses or other incentive plans, equity awards, pension or retirement benefits, a 401(k) company match, health and wellness programs, fitness centers, insurance benefits, paid time off, and family support benefits. Benefits may vary by country and role.

Requirements

• MD or equivalent advanced medical degree.
• Minimum of 4 years of clinical development experience in industry, including protocol design, study start-up, and study team execution.

Nice To Haves

• Clinical training in Internal Medicine, Endocrinology, or Cardiology; board certification or eligibility is strongly preferred.
• Experience with regulatory filings and health authority interactions.

Responsibilities

• Develop innovative clinical strategies to shorten development cycles in an evolving regulatory landscape.
• Design efficient, robust Phase 2/3 programs.
• Partner with discovery teams to inform next-generation targets and lead Phase 1 clinical testing plans for initial PK/PD and safety characterization.
• Safeguard patient safety in clinical studies and support signal detection from post-marketing surveillance.
• Act as a medical expert and leader in interactions with external stakeholders.
• Plan and execute publication and clinical communication strategies, and contribute to key external presentations.
• Ensure the quality of clinical documents, including investigator brochures, protocols, study reports, and regulatory submission materials.

Benefits

• Annual bonuses or other incentive plans may be offered, depending on country and role.
• Equity awards may be offered, depending on country and role.
• Pension or retirement benefits may be offered, depending on country and role.
• 401(k) company match may be offered, depending on country and role.
• Health and wellness programs may be offered, depending on country and role.
• Fitness centers may be available, depending on country and role.
• Insurance benefits, including medical, dental, vision, life, and disability coverage, may be offered, depending on country and role.
• Paid time off may be offered, depending on country and role.
• Family support benefits may be offered, depending on country and role.

What This Job Offers

• Job Type: Full-time
• Career Level: Senior
• Education Level: Ph.D. or professional degree