Senior Expert Bimzelx; Germany

Make your mark for patients

We are looking for a Senior Real World Evidence Expert who is scientifically rigorous, strategically minded, and collaborative to join our Real‑World Evidence (RWE) team, helping to shape evidence generation strategies that support better decisions for patients, healthcare systems, and the broader scientific community. This position can be based in Brussels, Belgium;
Slough, UK;
Monheim, Germany or Atlanta, USA.

As Senior RWE Expert, you will be responsible for designing and delivering global real‑world evidence (RWE) studies that generate impactful insights across the product lifecycle. You will contribute to strategic decision‑making by developing evidence that supports research and development activities, regulatory requirements, payer needs, and clinical practice.

In this role, you will help drive the development of asset‑level RWE strategies, working closely with cross‑functional stakeholders to identify evidence gaps, generate meaningful insights, and advance innovative approaches to evidence generation. You will also contribute to the evolution of real‑world data capabilities and methodologies that strengthen UCB’s ability to address complex healthcare challenges.

You will work closely with RWE Strategy Leads, Epidemiology and Evidence Synthesis teams, Safety and Pharmacovigilance colleagues, Biostatisticians, Data Scientists, and external research partners. You will collaborate across global functions to ensure evidence generation activities are aligned with strategic priorities and deliver meaningful value to patients and stakeholders.

• Lead the design, execution, and delivery of complex global RWE studies on time and within budget.
• Develop study concepts, protocols, statistical analysis plans, and study documentation to support evidence generation objectives.
• Drive epidemiology, natural history, disease burden, comparative effectiveness, safety, and post‑launch evidence generation initiatives.
• Lead secondary data studies and represent RWE in primary data collection study teams.
• Collaborate with external vendors, academic researchers, and medical experts to ensure high‑quality study execution.
• Interpret and communicate study findings to both internal and external stakeholders.
• Support the development and execution of asset‑level RWE strategies and evidence plans.
• Identify and implement innovative study designs, advanced analytics methodologies, and new real‑world data sources.
• Contribute to scientific publications, abstracts, posters, presentations, and external communications.
• Act as a trusted subject matter expert, providing strategic guidance and championing scientifically robust methodologies.

• Master’s degree, PhD, MD, or equivalent qualification in epidemiology, outcomes research, health economics, biostatistics, life sciences, or a related discipline.
• Significant experience designing and delivering real‑world evidence studies using primary and/or secondary data sources.
• Strong expertise in epidemiology, pharmacoepidemiology, outcomes research, health economics, biostatistics, data science, or related quantitative disciplines.
• Experience working within pharmaceutical, biotechnology, consulting, or academic research environments.
• Excellent communication skills with the ability to translate complex evidence into clear and actionable insights.
• Passion for innovation, scientific excellence, and the application of emerging technologies, including AI‑enabled approaches within real‑world evidence generation.

Internal applicants should be in their current job for at least 12 months, must meet performance standards and are not on formal corrective/disciplinary process (PIP),…