In this role you will lead and coordinate real-world evidence activities to inform drug development, regulatory submissions, and commercialization. You will partner with the global RWE Strategy Lead to align scientific, technical, and business inputs, ensuring rigorous, timely, and cost-efficient study delivery. You'll design and interpret epidemiological research and advocate for data-driven decisions across integral teams. You will contribute to high-impact studies that strengthen product value propositions and patient access.
Employee benefit programs
Competitive salary range disclosed
Diversity and inclusion actions
Global collaboration and development opportunities
Design, execute, analyze, and interpret epidemiological/outcomes studies to support regulatory submissions and development
Provide strategic epidemiological input and leadership to project teams across all stages of development
Deliver high-quality real-world research within time and budget constraints
Innovate study designs to address evidence gaps and support commercialization
Set standards for RWE utilization and provide methodological leadership
Identify and validate external data sources and partnerships for fit-for-purpose analyses
Maintain clear, timely communication with stakeholders to monitor progress and risk
Collaborate with cross-functional teams to optimize resources and outcomes
Minimum 7 years of real-world evidence generation in the pharmaceutical industry
Strong knowledge of RWE applications in development, regulatory, and patient access at international level
Understanding of product development processes across the lifecycle
Experience with innovative RWE methodologies to address evidence gaps
Experience across multiple therapeutic areas; transplant, diabetes, and cardiovascular experience preferred
Proven cross-functional collaboration in global matrix teams
Negotiation and interpersonal skills
Teamwork and collaboration
Pharmacoepidemiology, HEOR and RWE study designs and methodol
📌 Rwe Scientist (España)
🏢 Sanofi
📍 España