Medical Director, Clinical Development, Cardiology/Nephrology

Regeneron Pharmaceuticals; Tarrytown (GA); Sur place; USD 285 000 - 386 000; Plein temps

Résumé du poste

Regeneron Pharmaceuticals in Tarrytown, NY, seeks a Medical Director to lead cardiovascular/metabolic clinical development. You will act as Medical Lead for trials, design study concepts, and oversee protocols, collaborating with cross-functional teams to ensure scientific excellence and patient safety.

The role requires an MD with board eligibility or certification and at least 2 years in pharma or equivalent research, with potential regulatory submission experience. On-site work is expected.

Qualifications

• MD with board eligibility or board certification in Cardiology, Nephrology, or Neurology preferred; relevant experience acceptable.
• At least 2 years pharmaceutical industry experience (academic research acceptable).
• Experience with regulatory submissions (CTD/dossier) in ICH regions is an advantage.

Responsabilités

• Guide Global Clinical Study Team to deliver high-quality trials on time.
• Oversee medical monitoring of clinical trials to ensure patient safety and regulatory adherence.
• 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.
• Work with discovery teams to shape future targets and development opportunities.

Connaissances

MD degree

Board eligibility/certification

Clinical trial leadership

Formation

MD

Description du poste

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 regulatoryagencies or common technical document (CTD or "dossier") submission in an ICH region is an advantage

#MDJobs, #MDJobsCD, #Obesity, #SC

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 necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. 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/

Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on-site.

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