Allergy & Immunology Clinical Development Director

Regeneron Pharmaceuticals, Inc; Village of Tarrytown (NY); On-site; USD 200,000 - 320,000; Full time

Benefits offered by this job

Medical, dental and vision insurance

Life insurance and disability coverage

Global wellness support & benefits

Job summary

Regeneron Pharmaceuticals, Inc. is seeking a Medical Director, Clinical Development in Allergy & Immunology to lead clinical program deliverables, including protocols, regulatory documents and publications.

You will collaborate with Clinical Program Lead and cross-functional teams to shape development programs for early and late-stage assets. The role emphasizes leadership across studies, medical writing, and clear communication, with opportunities to travel to conferences and contribute to

Qualifications

• MD or equivalent; advanced clinical training in Allergy/Immunology strongly preferred.
• Understanding of drug development processes and regulatory requirements.
• Experience with clinical programs, protocols, and regulatory documents.

Responsibilities

• Provide clinical leadership for deliverables within a clinical program, including protocols and publications.
• Facilitate studies and support investigators on Regeneron-driven trials.
• Anticipate and resolve clinical and study conduct issues.
• Initiate and execute R&D programs for assets at different stages.
• Influence team decisions and align cross-functional teams.
• Communicate clearly through medical writing and presentations.
• Identify risks and propose mitigation strategies.
• Engage colleagues across levels with diplomacy and cultural awareness.

Skills

Clinical leadership

Study facilitation

Medical writing

Scientific communication

Regulatory understanding

Cross-functional collaboration

Risk mitigation

Diplomacy & stakeholder engagement

Education

MD or equivalent

Job description

Regeneron Pharmaceuticals, Inc. is seeking a Medical Director, Clinical Development in Allergy & Immunology to lead clinical program deliverables, including protocols, regulatory documents and publications.

You will collaborate with Clinical Program Lead and cross-functional teams to shape development programs for early and late-stage assets. The role emphasizes leadership across studies, medical writing, and clear communication, with opportunities to travel to conferences and contribute to