Project Toxicologist, Director - Oncology Targeted Delivery (OTD) Safety Science, Clinical Pharmacology and Safety Sciences (Cambridge, MA or Gaithersburg, MD)
$184.54k - $276.81kAstraZeneca
At AstraZeneca , our ambition is to eliminate cancer as a cause of death. Our pioneering oncology pipeline reflects this mission, and our Oncology Targeted Delivery (OTD) Safety team plays a critical role in advancing transformative therapies to patients. We are seeking a passionate and highly motivated Director, Project Toxicologist to join our OTD Safety group. This role will focus on novel targeted oncology therapies, including radioconjugates, antibody–drug conjugates (ADCs), and small molecules . Experience with radioconjugates is particularly valued; however, candidates with expertise in other relevant modalities are encouraged to apply. As a Project Toxicologist, you will partner with cross-functional teams across Oncology R&D, bridging discovery and regulatory toxicology. You will develop innovative safety strategies, guide candidate selection, inform regulatory approaches, and help shape the future of oncology safety science. LOCATIONS: Cambridge, MA (Kendall Square) or Gaithersburg, MD What you’ll do
- Lead toxicology strategies : Design and oversee regulatory and investigative toxicology programs to predict, assess, and mitigate target- and modality-related safety risks.
- Support development decisions : Apply your toxicology expertise to anticipate clinical safety risks and provide data-driven recommendations across discovery and development programs.
- Advance safety science : Integrate in vitro, in silico, and in vivo approaches with emerging technologies, including organ-on-chip, imaging, and omics, to address complex safety questions.
- Communicate integrated risk assessments : Present scientific conclusions and safety strategies to governance bodies and contribute to regulatory submissions.
- Provide regulatory and scientific leadership : Maintain and expand expertise in regulatory standards, preclinical safety, and modality-specific toxicology while anticipating industry trends and evolving methodologies.
- Support external opportunities : Provide strategic toxicology input for in-licensing evaluations, due diligence activities, and external collaborations.
- Build scientific influence : Advance Oncology Safety science through internal and external collaborations, publications, conference participation, and thought leadership.
- Develop people and partnerships : Contribute to an inclusive, collaborative environment and support the development of colleagues across teams and geographies.
- Education : PhD, DABT, or an advanced university degree in toxicology, pharmacology, oncology, or a related scientific discipline, together with a strong scientific track record.
- Professional experience : 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.
- Alternative experience pathway : 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.
- Oncology expertise : Deep understanding of oncology drug discovery and development, with a demonstrated ability to deliver toxicology programs supporting IND filings and broader development milestones.
- Modality expertise : Experience with radioconjugates or ADCs is preferred. Familiarity with small-molecule oncology therapeutics is also valuable.
- Translational safety skills : Experience applying in vitro, in silico, and in vivo tools to predict and characterize potential clinical safety risks.
- Leadership and collaboration : Ability to coordinate multiple projects across functions and geographies while working effectively in a complex, matrixed environment.
- Communication and influence : Strong scientific communication, interpersonal, and influencing skills, with the ability to inform decisions among scientific, clinical, and regulatory stakeholders.
- Commitment to inclusion : Demonstrated commitment to inclusion, diversity, collaboration, and team development, consistent with AstraZeneca’s Great Place to Work objectives.
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