Role Summary
Head, Center of Oncology Data Excellence (CODE) to lead cross-brand, cross-tumor data strategy and advanced analytics within Global Medical Affairs Oncology, embedding GenAI methodologies to deliver trusted, reproducible, globally scaled evidence for patients and the business.
Responsibilities
- Lead CODE Strategy: Define and implement a unified approach across Data Analytics, Global Data Strategy, Biostatistics, and Scientific Medical Writing.
- Work closely with stakeholders in EG2P and GMA to ensure research is timely and scientifically rigorous.
- Data Innovation: Oversee in-house RWE studies and other analyses to highest scientific standards.
- Scale Analytics Globally: Deliver coordinated capabilities that reduce cycle times and improve reproducibility across brands and regions/therapeutic areas.
- Data Strategy: Oversee global data strategy; review and purchase decisions for multiple data assets in partnership with stakeholders across EG2P and AZ.
- Delivery excellence: Ensure robust design, analysis, and interpretation for GMA-led trials, externally sponsored research (ESRs), and RWE/RWD studies including governance.
- Scientific Medical Writing: Lead development and QC of SDCs, protocols, study reports, abstracts and presentations leveraging GenAI tools when appropriate.
- Accelerate GenAI Adoption: Champion responsible GenAI deployment with guardrails, metrics, and human-in-the-loop validation; improve analytics and writing with GenAI capabilities.
- Drive End-to-End Integration: Align cross-functional teams from study build to evidence dissemination.
- Methods and tooling: Advance modern analytics (e.g., causal inference, target trial emulation, synthetic controls, time-to-event modeling), statistical computing practices (R/Python), and GenAI copilots to improve reproducibility and throughput.
- Standardise Excellence: Develop shared playbooks and reusable assets to accelerate delivery and ensure consistency.
- Governance & Compliance: Co-lead data and AI governance forums to meet regulatory expectations and inspection readiness.
- Infrastructure Leadership: Oversee development of scalable data environments and pipelines.
- Capability Building: Champion continuous learning in GenAI, advanced statistics, and data engineering.
- Programme Delivery: Own CODE milestones, delivery plans, and risk management across global programmes.
- Impact Measurement: Quantify business and patient impact through insights delivered and publications enabled.
Impact Expectations
- Elevate CODE as the enterprise center of excellence for oncology analytics, biostatistics, data strategy, and scientific medical writing.
- Deliver an integrated data and analytics strategy across brands and regions that reduces cycle times, improves reproducibility, and increases actionable insights.
- Operationalize GenAI across CODE with measurable productivity and quality gains, robust governance, and human-in-the-loop validation.
- Enable faster, higher quality evidence to inform publications and global medical strategies.
Required Qualifications
- PhD, MD, PharmD, or MS in outcomes research, epidemiology, biostatistics, epidemiology outcomes research, statistics, data science, or related field.
- 10+ years in pharma/biotech or health data, leading sophisticated analytics and evidence programmes; recognized authority in oncology and real-world research.
- Leadership: Advanced skills in team leadership, matrix management, stakeholder influence, and crossfunctional program delivery; excellence in vendor oversight and multisector collaboration.
- Communication: Outstanding written and verbal communication; ability to translate complex methods and trends into actionable strategies and compelling scientific outputs.
- Strong in RWE/RWD methods, study design, biostatistics, and R/Python; familiar with modern analytics engineering.
- Deep understanding of data integration, privacy standards (HIPAA, GDPR), and operationalizing compliant AI/ML/GenAI.
- Validated use of GenAI to improve analytics and scientific writing with measurable impact.