Medical Director, Clinical Development, Cardiology/Nephrology

Regeneron Pharmaceuticals, Inc.; New York (NY); On-site; USD 285,000 - 386,000; Full time

Job summary

Regeneron Pharmaceuticals, Inc. invites a Medical Director to join the Cardiovascular/Renal/Metabolism team in the Clinical Development Unit.

The role focuses on medical leadership for trials, designing study concepts, and overseeing protocols while collaborating with cross-functional partners. A physician scientist with strong clinical and scientific knowledge is expected to guide study concepts and oversight.

Qualifications

• MD or equivalent medical degree with board eligibility or certification in Cardiology, Nephrology, or Neurology (Autonomic specialists) preferred.
• Minimum 2 years pharmaceutical industry experience or equivalent in academia.

Responsibilities

• Lead Global Clinical Study Team to deliver high-quality trials on time.
• Oversee medical monitoring of clinical trials to ensure patient safety and regulatory compliance.
• Lead clinical study and protocol development and present to internal and external stakeholders.
• Provide clinical and scientific leadership for data review, study reports, and publications.
• Collaborate with cross-functional partners to advance program goals and deliverables.
• Coordinate with discovery teams to shape future targets and development opportunities.

Education

MD/DO or equivalent

Board-certified/board-eligible in Cardiology or Nephrology or Neurology

Job description

Build our future together:

At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Medical Director to join our Cardiovascular/Renal/Metabolism team supporting our Clinical Development Unit. In this role, you will serve as Medical Lead for clinical trials and are responsible for the design of clinical study concepts leading to clinical trial protocols and oversight of studies, while collaborating with cross-functional stakeholders. This role requires a high-performing and highly passionate physician scientist who serves as a clinical role model for the team and demonstrates outstanding clinical scientific knowledge applicable to clinical research.

This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.

When & where:

• Location: Tarrytown, NY
• Travel: 10% to relevant conferences

Discover your role:

• You guide the Global Clinical Study Team to deliver high-quality trials on time.
• You oversee the medical monitoring of clinical trials to ensure patient safety and adherence to regulatory guidance.
• You lead clinical study and protocol development and present to internal and external stakeholders.
• You provide clinical and scientific leadership for data review, study reports, and publications.
• You work closely with cross-functional partners to advance program goals and key deliverables.
• You collaborate with discovery teams to help shape future targets and development opportunities in the field.

This role requires:

• An M.D. or equivalent with board eligibility or board certification in Cardiology, Nephrology, or Neurology (Autonomic specialists) strongly preferred; relevant experience can be acceptable.
• At least 2 years pharmaceutical industry experience (equivalent research in academia will be considered)
• Previous interactions with regulatory agencies or common technical document (CTD or "dossier") submission in an ICH region is an advantage

#MDJobs, #MDJobsCD, #Obesity, #SC

We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.

Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other locations, additional information will be provided during the recruitment process.

As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.

For jobs in Canada: this posting is for an existing position.

Salary Range (annually)

$284,900.00 - $385,700.00