Senior Medical Director, Hematology/Oncology Clinical Dev

Regeneron Pharmaceuticals; Tarrytown (GA); On-site; USD 333,000 - 451,000; Full time

Job summary

Regeneron Pharmaceuticals seeks a Senior Medical Director to lead clinical development in Hematology/Oncology, directing deliverables across trials and regulatory submissions within a global framework.

Location options include Tarrytown, NY or Warren, NJ with on-site work four days a week; travel ~10% to conferences. MD or equivalent with 4+ years in industry clinical research is required.

Qualifications

• MD or equivalent medical degree, with hematology/oncology training preferred.
• 4+ years of industry clinical research experience across Phases 1–4.
• Strong understanding of global regulatory environments.
• Experience with start-up, conduct, and close-out of trials.

Responsibilities

• Manage all operational aspects and drive execution of clinical programs, in partnership with global line functions, the assigned Clinical Scientist, and Clinical Operations associates, to ensure timely execution of assigned clinical deliverables within approved budget.
• Lead interactions with external stakeholders (e.g., regulatory authorities, key opinion leaders, advisory boards, patient advocacy groups) and internal stakeholders (e.g., Research, Early Clinical Development, Medical Affairs, Marketing, HEOR), as well as internal decision boards.
• Ensure the overall safety of the compound in collaboration with the Safety Lead for the assigned program
• Lead development of clinical sections of program-level regulatory documents, such as Investigators' Brochures, briefing books, safety updates, and IND/NDA submission documents, and lead responses to Health Authority questions

Skills

Regulatory knowledge

Clinical trial operations

Leadership

Global teamwork

Education

MD or equivalent medical degree

Job description

Regeneron Pharmaceuticals seeks a Senior Medical Director to lead clinical development in Hematology/Oncology, directing deliverables across trials and regulatory submissions within a global framework.

Location options include Tarrytown, NY or Warren, NJ with on-site work four days a week; travel ~10% to conferences. MD or equivalent with 4+ years in industry clinical research is required.