Senior Medical Director

Build Our Future Together

The Senior Medical Director, Clinical Development provides clinical leadership and is responsible for all clinical deliverables within the assigned section of a clinical program in Hematology Oncology with minimal supervision from Program Lead MD. Clinical deliverables may include individual protocols consistent with the Clinical Development Plans (CDP); clinical components of regulatory documents/registration dossier and brand related medical information, clinical communications and publications. This position offers the opportunity to give to a fast-growing, science-driven organization making a significant difference to patients worldwide.

When & Where

• Location: Tarrytown, NY or Warren, NJ
• Work model/flexibility: 4 days a week on-site
• Travel percentage: 10% to relevant congresses/conferences

Discover Your Role

• Manages all operational aspects and drives execution of clinical programs in partnership with global line functions, assigned Clinical Scientist and Clinical Operations associates to ensure timely execution of assigned clinical deliverables within approved budget.
• Leads interactions with external stakeholders (e.g., regulatory authorities, key opinion leaders, advisory boards, patient advocacy groups), internal stakeholders (e.g., Research, Early Clinical Development, Medical Affairs, Marketing, HE&OR), and internal decision boards.
• Ensures overall safety of the compound in collaboration with the Safety Lead for the assigned program.
• Contributes to CRFs, outsourcing specifications, data monitoring and validation plans, analysis plan for all trials to ensure consistency within the program.
• Leads development of clinical sections of program level regulatory documents such as Investigators’ Brochures, briefing books, safety updates, IND/NDA submission documents, responses to Health Authorities questions with minimal input from Program Lead MD.

This Role Requires

• A M.D. degree, preferably with clinical training in a relevant disease area.
• More than 4 years’ demonstrated experience in clinical research or drug development in an industry environment spanning clinical activities in Phases 1 through 4.
• Understanding of global regulatory environment including key regulatory agencies and approval processes.
• A strong understanding of operational aspects of all phases of clinical trial conduct (start-up, conduct, close-out).
• People Management experience preferred but not required.

Salary Range (annually)

$333,300.00 - $450,900.00

Regeneron offers a competitive and comprehensive total rewards package which may include annual bonuses, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits, paid time off, and family support benefits.

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.