Immunology Medical Director, Clinical Development Leader

Regeneron Pharmaceuticals; Tarrytown (GA); On-site; USD 285,000 - 386,000; Full time

Job summary

Regeneron Pharmaceuticals seeks a Medical Director, Clinical Sciences to provide clinical leadership for assigned studies and drive program deliverables. This role requires an MD with a subspecialty fellowship and 0–4 years in industry clinical development, plus strong GCP knowledge and medical writing ability.

Based in Tarrytown, NY, you will contribute to protocols, regulatory documents and publications, and work within a matrix environment with cross-functional teams.

Qualifications

• MD degree with specialized clinical fellowship in Allergy/Immunology, Pulmonology, Dermatology or Infectious Diseases.
• 0-4 years of industry clinical development experience (academic research accepted).
• Strong knowledge of drug development, GCP, study design, and regulatory landscape in pharma.
• Advanced analytical/presentational skills with proficient medical writing.

Responsibilities

• Provide clinical leadership and own all clinical deliverables for an assigned section of a clinical program
• Facilitate assigned studies and provide investigator support for Regeneron-driven studies
• Anticipate and resolve study clinical issues as a trusted resource to the team
• Initiate and design development programs for early- and late-stage assets
• Ensure the medical science behind study concepts is accurate through reviews and expert consultation
• Contribute clinical content to protocols, regulatory documents and publications
• Identify critical risks and develop mitigation strategies
• Lead within a matrix environment with diplomacy and collaboration

Skills

Clinical leadership

Study design

Medical writing

Communication skills

Analytical skills

Presentation skills

Education

MD degree with subspecialty fellowship in Allergy/Immunology/Pulmonology/Dermatology or Infectious Diseases

Job description

Regeneron Pharmaceuticals seeks a Medical Director, Clinical Sciences to provide clinical leadership for assigned studies and drive program deliverables. This role requires an MD with a subspecialty fellowship and 0–4 years in industry clinical development, plus strong GCP knowledge and medical writing ability.

Based in Tarrytown, NY, you will contribute to protocols, regulatory documents and publications, and work within a matrix environment with cross-functional teams.