Medical Director, Clinical Development, Solid Tumor Oncology

Regeneron Pharmaceuticals, Inc.; Village of Tarrytown (NY); Vor Ort; USD 285.000 - 386.000; Vollzeit

Zusammenfassung

Regeneron Pharmaceuticals, Inc. is seeking a Medical Director, Clinical Sciences to lead oncology trial activities in solid tumours and ovarian cancer programs.

You will design study concepts, supervise trials, and guide the Clinical Team to meet milestones while partnering with Clinical Project Managers and Therapeutic Area leads. The role requires an MD or MD/PhD with at least 2 years of industry or academic research experience, and oncology fellowship training is strongly preferred.

Qualifikationen

• MD or MD/PhD with minimum 2 years of relevant research experience
• Oncology fellowship training preferred and translational/clinical research experience desirable
• Experience designing clinical study concepts and supervising clinical trials
• Ability to lead clinical teams and collaborate with project managers and therapeutic-area leads

Aufgaben

• Define clinical trial goals and objectives
• Inform trial design through literature and database research
• Collaborate with Clinical Project Managers, Trial Managers and Therapeutic Area Program Managers
• Lead the Clinical Team to achieve program milestones on schedule
• Engage with investigators and clinical study teams through meetings and committees

Kenntnisse

Leadership

Clinical trial oversight

Literature review

Cross-functional collaboration

Ausbildung

MD or MD/PhD

Oncology fellowship training

Jobbeschreibung

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, Clinical Sciences to join our Oncology team, supporting solid tumour drug development, including studies in ovarian cancer. In this role, you will design clinical study concepts, oversee the medical and scientific supervision of clinical trials, and lead the Clinical Team to deliver high‑quality program milestones, while collaborating with Clinical Project Managers, Clinical Trial Managers, and Therapeutic Area Program Managers. 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

• Define clinical trial‑related goals and objectives
• Conduct literature and database research to inform trial design
• Collaborate with Clinical Project Managers, Clinical Trial Managers, and the Therapeutic Area Program Manager
• Contribute to program team meetings, scientific advisory boards, study steering committees, and data/safety monitoring meetings
• Lead and supervise the Clinical Team to deliver high‑quality program milestones on schedule
• Build and maintain relationships with key study investigators

This Role Requires

• MD or MD/PhD with a minimum of 2 years of relevant research experience in industry or the academic research setting
• Oncology clinical fellowship training with translational and/or clinical research experience strongly preferred

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.

Salary Range (annually)

$284,900.00 - $385,700.00

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/. For other locations, additional information will be provided during the recruitment process.

If you have any questions, please speak with your recruiter.

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. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.

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.