Jobs at AstraZeneca PLC

Lead U.S. Commercial IT and Marketing Technology strategy, unifying CRM, MarTech, web, analytics, and omnichannel platforms. Shape roadmap, governance, and platform consolidation; manage a multidisciplinary team; drive cross-functional program delivery, adoption of advanced analytics/AI, vendor and stakeholder management, and continuous improvement to support commercial, marketing, and patient engagement.

Lead global clinical development and execution for hematology therapies (primarily CLL), including strategy, regulatory submissions, integrated product plans, budgets, timelines, and cross-functional team leadership. Build differentiated clinical plans, support governance and investment decisions, mentor teams, and coordinate internal and external stakeholders across early and late-phase trials.

Lead epidemiology strategy and execution across therapeutic areas; direct RWE and observational studies; advise clinical, regulatory, and safety teams; build and mentor epidemiology teams; drive methodological excellence, publications, and external scientific engagement.

Lead global regulatory strategy and operational regulatory activities for CVRM drug development programs. Serve as global or regional regulatory lead, shape clinical strategy, engage major health authorities, and support development, approval, launch, and lifecycle management of small and large molecule products.

Lead design and implementation of bioanalytical strategies (PK, PD, immunogenicity, biomarkers) for oncology programs. Serve as IBA project lead, collaborate with internal and CRO labs, provide scientific oversight for assays and regulatory submissions, mentor staff, and represent IBA externally through presentations and publications.

Lead development of analytical methods, formulations, and drug-delivery systems for small-molecule projects. Serve as pharmaceutical expert on global cross-functional teams, design and run experiments, interpret and present data, innovate new formulation technologies, and influence project strategy to advance investigational medicines.

Provide statistical expertise for complex clinical study design, analysis, modelling and simulation, and regulatory submissions. Develop statistical analysis plans, produce analyses, tables and graphics, coach junior statisticians, contribute to regulatory responses and publications, and identify methodological or process improvements to enhance study design and delivery.

Lead and develop a biostatistics team to design, deliver, and interpret statistical analyses for product development, regulatory submissions, and HTA. Ensure statistical quality, partner with CROs, represent externally, mentor staff, and promote novel methodologies while contributing to governance and cross-functional decision-making.

Lead global regulatory strategy for complex oncology programs, manage Global Regulatory Strategy Team, represent Regulatory on product teams, drive regulatory milestone delivery and risk mitigation, lead major health authority interactions and labeling negotiations, promote novel regulatory initiatives, and build external stakeholder relationships to support global approvals and competitive labeling.