RWE Senior Expert - Special Patient Populations

Make your mark for patients

We are looking for a RWE Senior Expert – Special Patient Populations who is collaborative, solutions-oriented, and passionate about leveraging real world data to improve the patient experience to join our Global Real World Evidence Team. This role can be based in Europe, either at our headquarters in Brussels, Belgium, or at one of our primary hubs in Monheim, Germany or Slough, United Kingdom.

The position is also available in multiple locations across the United States. This hybrid role requires a minimum of 40% on-site presence and 5‑10% domestic and international travel.

You will lead the design and execution of global real‑world evidence programs that generate insights to support research and development, guide strategic business decisions, advance understanding of disease and patient outcomes, and fulfill post‑market requirements. Your work will help inform decision‑making for a wide range of stakeholders, including patients, healthcare professionals, regulators, policymakers, and payers. A key focus of this role is generating evidence and developing real‑world data capabilities for special patient populations, including women of childbearing age, pediatric patients, and older adults, to address critical clinical, regulatory, and healthcare decision‑making needs.

You will be responsible for developing and strengthening real‑world data capabilities across specific disease areas, with a particular focus on women of childbearing age and other specialized patient populations, including pediatric and elderly patients. Working closely with cross‑functional partners, you will also shape and deliver the overarching real‑world evidence strategy for key development and commercial assets.

you will work closely with colleagues across Clinical Development, Medical Affairs, Drug Safety and Pharmacovigilance, Regulatory Affairs, Health Economics and Outcomes Research, Market Access, Biostatistics, Data Science, Evidence Generation, and Asset Strategy teams to develop and deliver evidence strategies that support decisions across the product lifecycle.

you will partner with academic researchers, healthcare providers, key opinion leaders, healthcare data partners, contract research organizations, and regulatory stakeholders to generate high‑quality evidence, advance scientific understanding, and address critical clinical, regulatory, and market access questions.

• Lead the design and execution of global real‑world evidence studies that support research, development, regulatory, medical, market access, and business decision‑making.
• Develop evidence‑generation strategies for special patient populations, including individuals who are pregnant, pediatric populations, older adults, and other underrepresented patient groups.
• Deliver complex observational research programs using real‑world data and prospective data collection, ensuring scientific rigor, operational excellence, and timely execution.
• Partner with cross‑functional teams to identify evidence needs related to disease burden, treatment outcomes, safety, effectiveness, and patient care pathways across the product lifecycle.
• Translate study findings into actionable insights and communicate results to internal stakeholders, external partners, scientific audiences, and regulatory bodies.
• Collaborate with external experts, research partners, and healthcare data providers to advance innovative evidence‑generation approaches.
• Shape long‑term evidence strategies for priority assets and disease areas while identifying opportunities to leverage new data sources, advanced analytics, machine learning, and artificial intelligence.
• Serve as a trusted scientific advisor,…