Medical Director, Clinical Development, Solid Tumor Oncology

About the Role

The Medical Director, Clinical Sciences, Oncology is a qualified physician scientist with exceptional academic clinical trials experience, preferably in solid tumor Oncology drug development. This role drafts designs of clinical study concepts which lead to clinical trial protocols and is responsible for medical and scientific supervision of individual clinical trials. This role may work on studies in ovarian cancer.

Responsibilities

• Defines clinical trial-related goals and objectives.
• Conducts literature and database research on clinical trials as needed.
• Collaborates with Clinical Project Managers, Clinical Trial Managers at the study level, and with the Therapeutic Area Program Manager.
• Contributes to program team meetings, scientific advisory boards, study steering committees, and data/safety monitoring meetings.
• Leads and supervises the Clinical Team to produce high-quality program deliverables on schedule.
• Maintains and develops relationships with key study investigators.

Requirements

• MD or MD/PhD with a minimum of 3 to 5 years of relevant research experience.
• Oncology clinical fellowship training with translational and/or clinical research experience is strongly preferred.

Schedule

This role has a 4-day onsite minimum requirement in Tarrytown, NY.

Pay

Salary Range (annually): $284,900.00 - $385,700.00.

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.
• Family support benefits.

For additional information about Regeneron benefits in the U.S., visit Regeneron Total Rewards. For other locations, additional information will be provided during the recruitment process.