At a Glance
- Tasks: Lead nonclinical development programs and design toxicology studies with cross-functional teams.
- Company: Join a leading pharmaceutical company focused on innovative therapies.
- Benefits: Competitive salary, health benefits, and opportunities for professional growth.
- Other info: Dynamic work environment with opportunities to stay updated on scientific advancements.
- Why this job: Make a real impact in drug development and safety assessment.
- Qualifications: Advanced degree in pharmacology or toxicology with relevant industry experience.
The predicted salary is between 60000 - 80000 £ per year.
The Senior Toxicologist utilizes their scientific expertise and regulatory experience to lead nonclinical development programs with guidance from her/his 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.
The Sr.
Toxicologist will provide primary authorship of all regulatory documentation required for submission packages, demonstrating excellent problem‑solving and communication skills (written and verbal).
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.
Contributing 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., Ph D, DVM) in pharmacology, toxicology or closely related biological science along with 3-5 years relevant pharmaceutical industry experience, or a Master's Degree + at least 10 years relevant pharmaceutical industry experience.
- Experience in designing, monitoring and interpreting non‑clinical safety studies.
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Senior Toxicologist in Cambourne employer: Regeneron Pharmaceuticals, Inc
At Regeneron, we pride ourselves on being an exceptional employer, offering a dynamic and inclusive work culture that fosters innovation and collaboration. As a Senior Manager in our Global Development Quality Assurance team, you will have the opportunity to lead impactful audit strategies while working remotely from the UK or Ireland, benefiting from a comprehensive rewards package that includes competitive bonuses, health and wellness programs, and robust employee growth opportunities. Join us in making a meaningful difference in patients' lives while enjoying a supportive environment that values diversity and professional development.
Contact Details:
Regeneron Pharmaceuticals, Inc Recruitment Team
