Senior Cell Therapy Clinical Development Leader

Regeneron Pharmaceuticals, Inc.; Village of Tarrytown (NY); Vor Ort; USD 333.000 - 451.000; Vollzeit

Benefits dieser Stelle

Annual bonuses

Equity awards

Pension benefits

401(k) match

Health benefits

Wellness programs

Insurance benefits

Paid time off

Family support benefits

Zusammenfassung

Regeneron Pharmaceuticals, Inc. seeks a Senior Medical Director to join the Hematology team supporting Cell Therapy Clinical Development. You will provide clinical leadership for all clinical deliverables within an assigned program, operating with minimal supervision from the Program Lead MD.

Location: Tarrytown, NY or Warren, NJ with up to 10% travel to conferences. You will lead external and internal stakeholder interactions, ensure safety, and drive regulatory document development across

Qualifikationen

• MD or equivalent medical degree is required.
• 4+ years of clinical research experience in industry.
• Cell Therapy experience preferred.
• Strong understanding of global regulatory environment and approvals.
• Operational experience in all phases of clinical trials.

Aufgaben

• Manage operational aspects and drive execution of clinical programs.
• Lead interactions with regulators, KOLs, advisory boards and internal teams.
• Ensure overall safety of the compound with the Safety Lead.
• Develop clinical sections of program regulatory documents and respond to health authority questions.

Kenntnisse

Stakeholder management

Leadership

Clinical operations

Regulatory understanding

Ausbildung

MD or equivalent medical degree

Clinical training in Hematology/Oncology

Jobbeschreibung

Regeneron Pharmaceuticals, Inc. seeks a Senior Medical Director to join the Hematology team supporting Cell Therapy Clinical Development. You will provide clinical leadership for all clinical deliverables within an assigned program, operating with minimal supervision from the Program Lead MD.

Location: Tarrytown, NY or Warren, NJ with up to 10% travel to conferences. You will lead external and internal stakeholder interactions, ensure safety, and drive regulatory document development across