Make your mark for patients
We are looking for a Senior Real World Evidence Expert who is scientifically rigorous, strategically minded, and passionate about generating impactful real‑world evidence to help shape key decisions across the lifecycle of UCB’s assets, based in Slough, UK or Brussels, Belgium
About the Role
As a Senior RWE Expert, you will autonomously design, lead, and deliver a wide range of global real‑world evidence (RWE) studies. Your work will inform internal decision-making, support regulatory and payer interactions, and contribute to the scientific understanding of disease areas. In addition to overseeing project delivery, you will help shape asset‑level RWE strategies and propose innovative approaches to evidence generation in partnership with the RWE Strategy Lead.
Who You’ll Work With
You will collaborate with statistical teams, RWE Analysts, epidemiologists, clinical teams, Evidence Synthesis partners (HE/HTA), Safety/Pharmacovigilance, external vendors, medical experts, and cross‑functional asset teams. You will serve as an influential scientific contributor with the ability to engage diverse stakeholders and ensure RWE outputs meet strategic, regulatory, and scientific needs.
What You’ll Do
1. Lead execution of complex global RWE studies using diverse methodologies and datasets end‑to‑end.
2. Develop study concepts, write protocols, shape analysis plans, and ensure governance and QC compliance.
3. Deliver epidemiology, natural‑history, burden‑of‑disease, safety‑outcome, regulatory, and comparative‑effectiveness studies.
4. Represent RWE on primary data‑collection teams and lead high‑visibility secondary data‑use initiatives.
5. Collaborate with vendors, clinicians, statisticians, and analytics teams to deliver scientifically robust outputs.
6. Interpret results and communicate findings internally and externally across scientific and strategic forums.
7. Co‑define evidence needs with HE/HTA partners, Safety, and other functions to support regulatory and payer interactions.
8. Contribute to asset‑level RWE strategy and propose innovative study designs, data sources, and analytic approaches.
9. Advocate for rigorous scientific methodology and challenge assumptions using strong methodological reasoning.
10. Help advance RWE functional excellence through thought leadership, innovation, and best‑practice sharing.
Interested? For this role we’re looking for:
11. Master’s degree, PhD, or MD in a life science, epidemiology, outcomes research, HEOR, statistics, or related field.
12. Experience designing and delivering RWE studies using primary or secondary data in pharma, academia, or consultancies.
13. Strong quantitative and methodological expertise across epidemiology, pharmacoepidemiology, and outcomes research.
14. Ability to develop high‑quality scientific communications (abstracts, manuscripts, posters, presentations).
15. Excellent communication skills with the ability to influence and engage cross‑functional and senior stakeholders.
16. Proven ability to lead projects independently, think strategically, innovate, and adapt in fast‑changing environments.
Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!