Clinical Pharmacology Lead, Oncology Programs

Regeneron Pharmaceuticals, Inc.

Warren (MI)

On-site

USD 176,000 - 287,000

Full time

11 days ago

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Job summary

Regeneron Pharmaceuticals, Inc. seeks an Associate Director to lead our Clinical Pharmacology group. You will provide strategic and scientific expertise, represent the function at meetings, and support oncology programs across development stages.

You will design and oversee PK/PD analyses, mentor junior scientists, and contribute to clinical study reports and regulatory submissions. Location options include Tarrytown NY, Warren NJ, or Cambridge MA, with a four‑day onsite work model.

Qualifications

  • PhD required with 8+ years of relevant Clinical Pharmacology experience.
  • Ability to design and oversee PK/PD analyses for clinical programs.
  • Strong communication of complex strategies to cross‑functional teams.
  • Experience with preparation of clinical study reports and regulatory submissions.

Responsibilities

  • Proactively identify and contribute significant clinical pharmacology insights for R&D programs, addressing strategic needs and regulatory hurdles.
  • Communicate complex strategies and results to development teams in an influential manner.
  • Independently design or oversee analyses and inform management of results and issues promptly.
  • Mentor staff and provide scientific leadership in clinical pharmacology.
  • Prepare timely, accurate clinical study reports and regulatory submission documents.

Skills

Clinical pharmacology
PK/PD analysis
Mentorship
Regulatory knowledge

Education

PhD in Biology, Pharmacology, Engineering, Pharmacy (Pharm.D.) or Medicine (MD)

Job description

Regeneron Pharmaceuticals, Inc. seeks an Associate Director to lead our Clinical Pharmacology group. You will provide strategic and scientific expertise, represent the function at meetings, and support oncology programs across development stages.

You will design and oversee PK/PD analyses, mentor junior scientists, and contribute to clinical study reports and regulatory submissions. Location options include Tarrytown NY, Warren NJ, or Cambridge MA, with a four‑day onsite work model.

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