Principal Toxicologist

Regeneron · Tarrytown

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ResearchFull-time$151k–$246kCompany career page

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Role summary

Regeneron seeks a Principal Toxicologist to lead nonclinical development programs within Drug Safety and Pharmacometrics. The role involves designing and overseeing toxicology studies, managing regulatory submissions, and collaborating across therapeutic areas with minimal supervision.

Where this listing comes from

This listing was compiled by RoleLantern from the employer's publicly available posting on Workday, captured and rephrased by RoleLantern using automated (AI) tools on 2026-10-02 (originally posted 2026-10-02). It was not submitted or confirmed by the employer through RoleLantern. Details may be inaccurate, incomplete, outdated, or no longer available; please confirm with the employer's official posting before applying.

What they're looking for

PhD, DVM, or Master's degree in Toxicology or related discipline
5+ years (PhD/DVM) or 15+ years (Master's) pharmaceutical industry experience
Expertise in design and oversight of nonclinical safety assessment studies
Experience contributing to regulatory submissions (INDs, CTAs, BLAs/MAAs)
Strong knowledge of global regulatory requirements and GLP, ICH, FDA, EMEA guidelines
Cross-functional drug development team experience as nonclinical safety lead

What you'll be doing

Represent toxicology on global R&D project teams and communicate nonclinical safety strategy
Develop regulatory risk assessments and oversee execution of toxicology studies
Provide scientific oversight of CRO activities including study design and data interpretation
Author and review nonclinical safety content for regulatory submissions
Mentor junior scientists and drive continuous improvement initiatives

Privacy & handoff

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Date posted1 day ago

Last source check1 day ago

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