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About the role
Key responsibilities & impact- Establish and execute RWE strategies across global therapeutic areas
- Translate medical needs into evidence supporting regulatory, access, and medical decisions
- Lead end-to-end planning and execution of real-world evidence strategies and studies
- Partner with Global Medical, Market Access, HEVA, and Global Brand Teams
- Build asset and brand RWE strategies aligned with global disease-area strategies
- Support GenMed medical gaps within Global Integrated Evidence Generation Plans
- Develop data strategies and assess data availability, access, and suitability
- Conduct data landscaping, assessment, and preparation for future indications and formulations
- Serve as a methodological expert in real-world study design and execution
- Deliver pre- and peri-launch support to prioritized countries
- Develop study budgets with internal and external stakeholders
- Manage study execution to ensure timely, in-budget, high-quality deliverables
- Influence matrix teams and optimize resources
- Communicate evidence strategy, study progress, risks, and mitigation plans
- Represent Sanofi’s RWE capabilities at scientific congresses and with regulatory bodies
- Contribute to building and transforming enterprise-level RWE capability and culture
Requirements
What you’ll need- Advanced degree in pharmaco-epidemiology, biostatistics, Health Outcomes, or equivalent discipline
- PhD preferred
- Formal education in business or management desirable
- At least 10 years of real-world evidence generation in or for the pharmaceutical industry
- End-to-end leadership of RWE studies from concept to completion and publication for regulatory or reimbursement submissions
- Experience using innovative RWE methodologies to address evidence gaps
- Significant peer-reviewed publication track record in epidemiology, clinical, statistical, and/or HEOR journals
- Experience working in multiple therapeutic areas; Immunology, Rare Diseases, Oncology, Neurology, or Ophthalmology experience highly valued
- Experience collaborating cross-functionally in complex global matrix teams
- Expertise in pharmacoepidemiology, HEOR, and RWE study designs and methodologies
- Experience working with routinely collected data, including claims databases, electronic medical health records, registries, and structured or unstructured healthcare data
- Ability to build evidence strategies from business needs and translate them into study requirements
- End-to-end project management of real-world studies and management reporting
- Working knowledge of commercial strategy, including market share, competitors, and product positioning
- Fluency in spoken and written business English mandatory
- Proficiency or working knowledge of French or other European languages is a plus
Benefits
Comp & perks- Opportunities for career growth through promotion or lateral moves, at home or internationally
- Rewards package recognizing contribution
- Health and wellbeing benefits
- High-quality healthcare
- Prevention and wellness programs
- At least 14 weeks’ gender-neutral parental leave
- Patient insights incorporated into drug development
- Work with cutting-edge AI, data, and digital platforms