Medical Director, Clinical Development, Obesity

Regeneron Pharmaceuticals • Tarrytown, GA

1d • $284,900 - $385,700 • Onsite

About The Position

The Medical Director, Clinical Development, Obesity is a qualified physician with pharmaceutical industry experience, preferably in the area of metabolism, obesity, or Type 2 diabetes. This role serves as Medical Lead for clinical trials within the Clinical Development Program (CDP) and is responsible for the design of clinical study concepts leading to clinical trial protocols. The position requires a high-performing and passionate physician scientist who acts as a clinical role model for the team and demonstrates outstanding clinical scientific knowledge applicable to clinical research. Regeneron is a leading biotechnology company that invents life-transforming medicines for people with serious diseases. Founded and led for over 30 years by physician-scientists, Regeneron's unique ability to repeatedly and consistently translate science into medicine has led to nine FDA-approved treatments and numerous product candidates in development, almost all of which were homegrown in their laboratories. Their medicines and pipeline are designed to help patients with eye diseases, allergic and inflammatory diseases, cancer, cardiovascular and metabolic diseases, neurology, infectious diseases, and rare diseases. Regeneron is also proud of its award-winning culture of innovation, being recognized as a Great Place to Work in 2021, Fast Company’s Best Workplace for Innovators in 2020, and Forbes JUST companies in 2020, among others.

Requirements

• An M.D. or equivalent with board eligibility or board certification in Pediatric Endocrinology preferred; relevant experience can be acceptable
• At least 2 years pharmaceutical industry experience (equivalent research in academia will be considered)
• Experience in metabolic disorders drug development strongly preferred

Nice To Haves

• Previous interactions with regulatory agencies or common technical document (CTD or “dossier”) submission in an ICH region is an advantage

Responsibilities

• Acts as medical expert and leader in interactions with external stakeholders
• Defines clinical trial-related Clinical Development Program (CDP) goals and objectives
• Works closely with discovery teams to provide input on the next generation of targets in the field
• Responsible for the relevance and accuracy of medical science underpinning of clinical study concepts (CSC) based on thorough scientific review and consultation with internal and external experts
• Reviews and finalizes clinical study concepts for presentation to Therapeutic Head, Strategic Program Teams, and internal governance meetings
• Leads the Global Clinical Study Team to produce high quality program deliverables on schedule
• Responsible for the medical content of clinical study reports, the analysis of clinical data, including safety monitoring, and all activities and procedures that ensure patient safety

Benefits

• health and wellness programs (including medical, dental, vision, life, and disability insurance)
• fitness centers
• 401(k) company match
• family support benefits
• equity awards
• annual bonuses
• paid time off
• paid leaves (e.g., military and parental leave)

What This Job Offers

• Job Type: Full-time
• Career Level: Director
• Education Level: Ph.D. or professional degree
• Number of Employees: 5,001-10,000 employees