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About the role
Description supplied by the original job listing.
Location: Barcelona - Spain or Cambridge - UK (3 days in-office requirement)
About AstraZeneca and AISI
At AstraZeneca, technology and science meet to change what is possible for patients. We are building a connected, end-to-end Enterprise AI engine — uniting data foundations, AI technology, process reinvention, and business-facing AI to accelerate results across the whole value chain. Success depends on being exceptional connectors: you will actively leverage existing capabilities, celebrate and promote reuse, export breakthrough ideas across geographies and functions, and obsess over scaling impact rather than building in isolation.
AI Science & Innovation (AISI) sits at the centre of AstraZeneca's R&D AI transformation. Our remit is to build, buy, and deliver the AI models and agents that change pipeline outcomes across discovery, translational science, biomarkers, and clinical development.
Within AISI, the Clinical AI teams are building world-class AI capability to accelerate the design, conduct, and analysis of clinical trials across our BioPharmaceuticals pipelines — spanning both early and late phase programmes. We partner closely with clinical development, regulatory, and biometrics teams to bring better treatments to patients faster, while adhering to the highest evidentiary standards.
The Opportunity
Bringing new treatments to patients demands scientific excellence at every stage of development. In the Clinical AI team, we focus on one of the most data-rich and decision-intensive parts of that journey: clinical development. Trial design, patient selection, dose optimisation, biomarker strategy, and safety evaluation each represent genuine opportunities where AI and machine learning can add rigour, speed, and precision — not as a replacement for clinical and statistical expertise, but as a powerful complement to it. We hold ourselves to measurable standards of improvement, and we build methods that can be evaluated, reproduced, and trusted in regulatory settings.
You will work across the enterprise to define and deliver on AstraZeneca's most pressing clinical development questions — leading cross-functional teams spanning the key BioPharmaceuticals disease areas of cardiovascular, renal, metabolic disease, respiratory, immunology and cell-therapy. You and the team will develop reusable methods and enterprise-scale approaches that measurably advance the late-stage drug pipeline. This is a high-visibility opportunity to shape how AstraZeneca does AI for BioPharmaceuticals clinical development — from methodology standards to external scientific influence.
AI for clinical development is a field in motion. Foundation models, agentic systems, and causal AI are advancing rapidly, and the regulatory and methodological frameworks around them are evolving in parallel. As a Director, Data Scientist, you will define and drive the AI methodology agenda for one or more programmes within Clinical AI, leading by scientific influence and matrix coordination rather than through a formal hierarchy. You will be the scientific authority that study teams, biometrics, and regulatory colleagues turn to — and AstraZeneca's voice externally at the critical moment when the rules of the road for AI in clinical trials are being written.
Key Responsibilities
Define and drive the AI methodology roadmap for assigned Clinical AI programmes, spanning early and late phase clinical development, and aligning AI/ML priorities with clinical and business objectives.
Lead, by matrix influence and scientific authority, the delivery of the most complex and high-stakes AI projects — from problem definition and methodology selection through validation, regulatory alignment, and scaled adoption across the enterprise.
Develop and govern reusable, enterprise-grade AI methods and evaluation frameworks for clinical trial settings, including innovative trial design support, dose optimisation, biomarker discovery, digital twins, predictive and prognostic modelling, and safety and efficacy signal detection.
Champion data-centric AI practices at programme level: govern the acquisition, curation, and quality control of datasets for model training, post-training, benchmarking, and evaluation across clinical and regulatory settings.
Partner with Clinical Development, Biometrics, Regulatory, and Study Teams to embed AI strategy and validated solutions into study design and decision-making at programme level.
Shape the AI evidence component for regulatory submission packages; act as the scientific and methodological voice in regulatory engagements involving AI/ML methods or innovative trial designs (FDA, EMA, MHRA).
Evaluate and champion cutting-edge AI methodologies — including foundation models, agentic AI systems, generative patient models, multimodal learning, Bayesian inference, causal inference, and model calibration and domain adaptation — proposing fit-for-purpose approaches with robust evaluation criteria and risk assessment.
Establish and maintain external collaborations with academic institutions, technology partners, and industry consortia to access novel capabilities and advance the scientific agenda.
Represent AstraZeneca at scientific conferences, standards bodies, and peer-reviewed venues; contribute first- or last-author publications in leading ML and clinical AI journals.
Serve as a technical mentor and thought partner for Associate Directors and Senior Data Scientists within the Clinical AI team; promote scientific rigour, reuse, and a culture of learning in public.
Contribute to the broader AISI AI for Clinical Development strategy, including cross-functional ways of working, tooling governance, and methodology standards.
Essential Requirements
PhD in Computer Science, Machine Learning, Statistics, Mathematics, Biomedical Informatics, Computational Biology, or a closely related quantitative discipline — with a strong, hands-on computational track record.
4–8 years of post-PhD experience in AI and machine learning method development, with demonstrated and sustained impact in clinical, biomedical, or drug development settings (e.g. models delivered, first-author publications, patents, SaMD filings, open-source projects).
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