Rwe Scientist - Sanofi

Sanofi; Barcelona; Presencial; EUR 90.000 - 130.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Employee benefit programs

Competitive salary range disclosed

Diversity and inclusion actions

Global collaboration and development机会

Descripción de la vacante

Sanofi is seeking a senior Real-World Evidence (RWE) leader to design and coordinate global RWE studies that inform drug development, regulatory submissions, and commercialization. You will partner with the global RWE Strategy Lead to align scientific, technical, and business inputs, ensuring timely study delivery and data-driven decisions across international teams.

The role requires minimum 7 years in pharmaceutical RWE, strong methodological leadership, and experience with claims, EHRs, and

Formación

• 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 routinely collected data (claims, EHRs, registries) and diverse data sources.
• Ability to translate business needs into study and data requirements.

Responsabilidades

• 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.

Conocimientos

RWE expertise

Epidemiology

Leadership

Cross-functional collaboration

Communication

Negotiation

Teamwork

Data source evaluation

Descripción del empleo

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 global 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 methodologies
• Experience with routinely collected data (claims, EHRs, registries) and diverse data sources
• Ability to translate business needs into study and data requirements