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AstraZeneca

Global pharmaceutical company developing prescription medicines

Project Toxicologist - Multiple Teams

Biology & BiotechConfirmed live in the last 24 hours
Full-time

About the Job

Requirements

  • A PhD, DABT, or an advanced university degree in toxicology, pharmacology, oncology, or a related scientific discipline, together with a strong scientific track record.
  • Typically, at least 10 years of experience in project toxicology, investigative toxicology, regulatory toxicology, or related safety-focused roles within the pharmaceutical, biotechnology, or CRO sector.
  • Candidates with a minimum bachelor's degree and substantial additional pharmaceutical industry experience may also be considered, including candidates with approximately 15 or more years of relevant experience.
  • Deep understanding of oncology drug discovery and development, with a demonstrated ability to deliver toxicology programs supporting IND filings and broader development milestones.
  • Experience applying in vitro, in silico, and in vivo tools to predict and characterize potential clinical safety risks.
  • Ability to coordinate multiple projects across functions and geographies while working effectively in a complex, matrixed environment.
  • Strong scientific communication, interpersonal, and influencing skills, with the ability to inform decisions among scientific, clinical, and regulatory stakeholders.
  • Demonstrated commitment to inclusion, diversity, collaboration, and team development.

Responsibilities

  • Design and oversee regulatory and investigative toxicology programs to predict, assess, and mitigate target- and modality-related safety risks.
  • Apply toxicology expertise to anticipate clinical safety risks and provide data-driven recommendations across discovery and development programs.
  • Integrate in vitro, in silico, and in vivo approaches with emerging technologies, including organ-on-chip, imaging, and omics, to address complex safety questions.
  • Present scientific conclusions and safety strategies to governance bodies and contribute to regulatory submissions.
  • Maintain and expand expertise in regulatory standards, preclinical safety, and modality-specific toxicology while anticipating industry trends and evolving methodologies.
  • Provide strategic toxicology input for in-licensing evaluations, due diligence activities, and external collaborations.
  • Advance Oncology Safety science through internal and external collaborations, publications, conference participation, and thought leadership.
  • Contribute to an inclusive, collaborative environment and support the development of colleagues across teams and geographies.

Desired Qualifications

  • Experience with radioconjugates or antibody–drug conjugates (ADCs) is preferred.
  • Familiarity with small-molecule oncology therapeutics is valuable.

About the Company

AstraZeneca

Global pharmaceutical company developing prescription medicines

AstraZeneca develops and markets prescription medicines and vaccines worldwide, with a focus on oncology, cardiovascular/metabolic, respiratory, and infectious diseases. Its products work by targeting specific biological pathways or cells, using small-molecule therapies, biologics, and vaccines to treat diseases or prevent infections. It differentiates itself through its dual heritage from Sweden and the UK, a broad pipeline, and strong R&D and collaborations that move from discovery to patient access. Its goal is to improve people’s health by discovering, developing, and delivering medicines and vaccines to patients worldwide.

Company size
10,001+
Company stage
IPO
Headquarters
Cambridge, United Kingdom
Founded
1913

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