Real-World Evidence (RWE) Lead

Real-World Evidence (RWE) Lead   Role Purpose As Real-World Evidence (RWE) Lead, you will own the country RWE strategy and execution, ensuring high-quality, compliant generation and use of evidence to inform medical, market access and regulatory strategies, support patient-centric decisions and demonstrate the value of the company’s medicines and vaccines.   Key Responsibilities RWE Strategy and Planning • Develop the Egypt RWE strategy and portfolio plans aligned with global and regional RWE/HEOR and Medical Affairs priorities. • Identify evidence gaps, unmet needs and opportunities to inform clinical practice, access and policy. • Integrate RWE plans into medical and brand strategies to support lifecycle management and value communication.   RWE Project Leadership • Lead the design, planning and execution of observational studies, registries and database analyses in collaboration with global/regional teams and external partners. • Ensure robust methodologies, clinically relevant endpoints and high-quality data collection and analysis, aligned with internal standards and regulatory expectations. • Oversee study timelines, budgets and governance, ensuring projects are delivered on time, within scope and to quality.   Collaboration and Value Demonstration • Partner with Medical Affairs, Market Access, Regulatory, Commercial and RWE/HEOR teams to address evidence needs and support value propositions for payers and regulators. • Translate RWE findings into clear, actionable messages and materials for internal stakeholders and, where appropriate and compliant, for external audiences. • Contribute RWE inputs to dossiers, value messages and policy engagement activities.   Data, Governance and Compliance • Ensure full compliance with company policies, local regulations, data privacy requirements and ethical standards in all RWE activities. • Oversee data access, data quality, anonymisation and documentation for RWE studies and analyses. • Maintain inspection readiness for RWE studies and records, supporting audits and inspections as needed.   External Engagement and Partnerships • Build and maintain relationships with academic institutions, research networks, data providers and other evidence partners. • Engage scientific and policy stakeholders on RWE methodologies and findings, in line with codes and governance.   Capability Building and Training • Develop country RWE capability through training on RWE concepts, study design, analysis and interpretation for Medical, Access and other teams. • Mentor colleagues to strengthen internal expertise and ensure sustainable, high-quality RWE operations.   Required Qualifications and Experience • Advanced degree such as MSc, MPH or PhD in epidemiology, biostatistics, public health, health economics or quantitative Life Sciences. • PhD or equivalent in epidemiology or outcomes research is an advantage. • 7–10 years of experience in RWE, outcomes research, epidemiology or related fields in pharma/biotech, academia or research organisations. • Proven experience in designing, executing and interpreting observational studies and database analyses. • Cross-functional matrix experience; Egypt or similar-market experience strongly preferred.   Key Capabilities and Skills • Deep expertise in RWE methods, study design, statistics and the use of observational data. • Ability to translate complex quantitative findings into clear, actionable insights for diverse stakeholders. • Strategic thinking and strong business acumen combined with a patient-centric mindset. • Excellent communication, presentation and influencing skills. • High integrity, strong ethics and a robust compliance orientation. • Fluency in English and Arabic, spoken and written.   If you are a data-driven, m