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Senior Toxicologist

Job in Cambridge, Middlesex County, Massachusetts, 02140, USA
Listing for: Regeneron
Full Time position
Listed on 2026-07-23
Job specializations:
  • Research/Development
    Research Scientist, Clinical Research, Regulatory Compliance Specialist, Pharmaceutical Science/ Research
Salary/Wage Range or Industry Benchmark: 128600 - 210000 USD Yearly USD 128600.00 210000.00 YEAR
Job Description & How to Apply Below

The Senior Toxicologist utilizes their scientific expertise and regulatory experience to lead nonclinical development programs with guidance from their direct supervisor working effectively within cross‑functional project teams. The Sr. Toxicologist will demonstrate a thorough understanding of GLP regulations and FDA/EMEA/ICH nonclinical safety guidelines to independently lead the design, conduct, interpretation, and reporting of regulatory toxicology and/or exploratory pharmacology/toxicology studies in rodent and non‑rodent safety models.

Experience with multiple therapeutic modalities preferred, including antibody, oligonucleotide, and gene‑therapy products.

Job Responsibilities
  • Represent toxicology on global research and development project teams communicating non‑clinical safety assessment strategy.
  • Coordinate cross‑department execution of the experimental plan including program budgets, and timing of toxicology studies in relation to regulatory and clinical milestones.
  • Work with study monitoring group to coordinate, design, monitor, and report toxicology and safety pharmacology studies at contract research organizations.
  • Communicate toxicology study findings, including relevant interpretation, to project teams and management.
  • Contribute to non‑clinical sections of regulatory documents including IND and NDA submissions.
  • Maintain currency with GLP regulations and ICH, FDA and EMEA non‑clinical safety guidelines.
  • Keep up with the latest scientific developments by reading the current literature and attending conferences.
Job Requirements
  • Advanced degree (e.g. PhD, DVM) in pharmacology, toxicology or closely related biological science along with 3-5 years relevant pharmaceutical industry experience, or Master’s Degree + 10 years relevant pharmaceutical industry experience.
  • Experience in designing, monitoring and interpreting non‑clinical safety studies.

Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law.

Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.

Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits.

Salary Range (annually): $ - $

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Position Requirements
10+ Years work experience
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