Jobs at AstraZeneca

Lead global oncology Field Medical strategy and MSL excellence initiatives. Guide Field Medical Leadership Team, align global-to-local tactics, oversee clinical trial support, insights reporting, digital/CRM adoption, compliance, budget and vendor management, and mentor Associate Directors to build consistent, high-performing MSL capabilities across regions.

Lead US regulatory strategy and FDA engagement for oncology products across development and lifecycle. Drive NDA/SNDA submissions, prepare US dossiers and labeling, advise cross-functional teams on regulatory risk/mitigation, mentor regulatory team members, and represent US perspectives within global regulatory strategy.

Lead end-to-end creation of medically accurate visual assets (infographics, data visualizations, medical illustrations, slide decks, digital and video assets). Apply UX principles and enterprise design-system standards to build scalable, component-based web and omnichannel medical content. Mentor designers, manage multiple projects, ensure brand/compliance alignment, and produce Figma wireframes, prototypes, and reusable design components.

Lead global, medium-complexity projects and change initiatives across functions. Define governance, drive continuous improvement, manage stakeholder engagement, assess risks, ensure quality, and mentor junior team members to deliver business value.

Design, deploy, and operate production-grade Generative AI agents and GenAI workflows for clinical trial optimization. Build scalable cloud infrastructure, automate via IaC and CI/CD, integrate LLM routing and monitoring (latency, token usage, hallucination detection), and collaborate with AI engineers and data scientists to move models from research to reliable production services.

Design, validate, and deploy publication-grade predictive and causal models for commercial and patient outcomes in rare disease. Build survival and time-series models, Bayesian marketing-mix and next-best-action systems, integrate Snowflake Cortex AI and AI agents, ensure HIPAA-compliant data operations, implement interpretability and bias guardrails, and translate insights to commercial stakeholders.

Lead clinical development activities by translating disease strategy into study concepts and protocols, supporting trial design and execution (early and late phase), ensuring data integrity and regulatory submissions, engaging investigators and sites, collaborating cross-functionally, and upholding GCP and ethical standards to enable global registration and high-quality clinical study delivery.

Lead GI cancer brand strategy and execution, collaborate cross-functionally and with global counterparts, plan budgets, deploy customer activities and sales content, monitor sales and market trends, drive KEE relationships and advocacy, complete strategic business plans, and manage an intern.

Lead analytics and strategy for HCP engagement operations supporting rare disease commercial teams. Design and execute quantitative and qualitative analyses, build dashboards and Smartsheet controls, address data quality and integration, support CRM and vendor integrations, identify compliance risk trends, and deliver actionable insights to inform commercial decisions. Partner cross-functionally with Marketing, Sales, Compliance, and external vendors to drive process improvements and ensure audit-ready, policy-aligned operations.

Lead development and execution of market access strategies across product lifecycle to optimize public and private reimbursement. Advise on payer negotiations, coordinate cross-functional teams, identify evidence gaps, engage external partners, manage brand access budgets, mentor staff, and ensure adverse event reporting compliance.

Lead end-to-end radioconjugate manufacturing at a GMP facility, ensuring safe, compliant production for clinical and commercial supply. Oversee operations, quality, teams, process improvements, cross-functional transfers, capital projects, and radiation safety.

Designs, conducts, troubleshoots, and analyzes in vitro experiments to validate reagents, probe target biology, and define mechanisms for radioconjugate oncology programs. Supports cross-functional teams, generates preclinical datasets, presents results, and ensures GLP and safety compliance while working with radioisotopes.

Manage and analyze Market Access contract operations including master data, contracting, membership, chargebacks and rebates. Validate and update customer master data, ensure contract compliance, interpret contract language, coordinate with internal/external stakeholders, participate in cross-functional projects, and recommend process enhancements for claims systems.

Support design and tech transfer of manufacturing and analytical processes for targeted alpha therapies. Perform lab work, analyze data, lead technology transfers, produce SOPs and validation documents, participate in validation/qualification, and support CMC investigations.

Lead translation of AI strategy into scaled enterprise outcomes by partnering with senior leaders to shape use cases, prototype, and deploy AI solutions across end-to-end processes. Provide hands-on technical leadership (coding, model review, data pipelines), lead cross-functional delivery, ensure governance/Responsible AI/compliance, and build organizational AI capability and adoption.

Lead study-level clinical data management for oncology trials, overseeing vendors, EDC/database builds, quality, inspection readiness, standards adoption, timelines, budgets, and mentoring junior DM staff to deliver inspection-ready datasets for regulatory decisions.

Lead statistical design, simulation, analysis, and interpretation for late-stage oncology studies. Develop Statistical Analysis Plans, produce analyses/graphics/tables, apply simulation and advanced methods, and communicate results to multidisciplinary teams and regulators. Contribute to methodology and process improvements, support regulatory submissions and governance, and mentor peers while owning high-quality statistical deliverables and timelines.