Regulatory Toxicologist

Regulatory Toxicologist

• North Yorkshire - with potential hybrid/onsite working depending on project needs
  
  
• Up to £50,000 per annum plus benefits
  
  My client is a growing, science-driven Contract Research / Development lab based in Yorkshire, working with clients to support preclinical toxicology, safety assessment and regulatory submissions.
  
  Key Responsibilities
  
  
• Review, evaluate and interpret toxicology data (in vitro, in vivo, literature) for preclinical safety assessments.
  
  
• Design, oversee or coordinate toxicology and safety-pharmacology studies (outsourced or in-house) in compliance with regulatory and GLP/GCP standards.
  
  
• Prepare and compile toxicology / safety sections for regulatory dossiers (e.g. IND / CTA / IMPD / CTD / briefing documents), including hazard / risk assessments, weight-of-evidence reports, and data gap analyses.
  
  
• Liaise with external CROs, clients, internal project teams (R&D, regulatory affairs, project management) to coordinate study plans, timelines and deliverables.
  
  
• Provide scientific advice on testing strategy, toxicological risk, and regulatory compliance throughout non-clinical development.
  
  
• Maintain up-to-date knowledge of regulatory guidelines and scientific developments; ensure compliance with relevant frameworks.
  
  
• Peer-review work, supervise or mentor junior scientists / toxicologists, and contribute to project- and lab-level safety strategy.
  
  
• Communicate findings internally and to external stakeholders / clients; produce clear, high-quality reports and regulatory-ready documents.
  
  The Regulatory Toxicologist will have:
  
  
• MSc / PhD (or equivalent) in Toxicology, Pharmacology, Biomedical Sciences, Biochemistry, or related life-science discipline.
  
  
• Solid experience in toxicology, safety pharmacology or non-clinical safety assessment — ideally within a pharmaceutical, biotech or CRO environment.
  
  
• Familiarity with in vitro and/or in vivo toxicology methods, ADME/TK, genotoxicity, safety pharmacology or related toxicity endpoints.
  
  
• Strong understanding of regulatory requirements, guidelines (e.g. ICH, GLP), and dossier preparation processes.
  
  
• Excellent scientific writing and communication skills; ability to produce regulatory-quality reports.
  
  If this sounds like you then please apply today