PpWe are looking for a bPrincipal Statistician /b to join us in our bBiometrics Data Science /b team, to be based in any of our Brussels (Belgium), Monheim (Germany), Slough (UK) or Raleigh (US) offices. /ph3Overview /h3h3About The Role /h3pYou will be supporting late‑stage drug development across one or more programs. This is a high impact role for a statistician who values ownership, collaboration, and using data to enable confident development decisions and support regulatory submissions. /ppYou will act as a key contributor, representing BDS within cross‑functional development teams, partnering closely with clinical, regulatory, and biometrics colleagues to shape strategy, deliver high‑quality outputs, and ensure our trials are decision‑ready, regulator‑ready, and inspection‑ready. /ph3What You’ll Do /h3ulliProvide statistical leadership for one or more indications or compounds, with a focus on Phase 2/3 and late‑stage development /liliAct as a trusted biometrics partner within cross‑functional program teams, influencing development and regulatory strategy /liliTake accountability for high‑quality statistical deliverables, including study design input, DMC activities, analyses, and regulatory‑facing outputs /liliTranslate development objectives into robust, practical, and innovative quantitative solutions /liliWork closely with the Project Lead Statistician, Clinicians, Programmers, and Regulatory colleagues to enable timely, informed decision‑making /liliIdentify risks and opportunities early, contributing thoughtfully to solutions /li /ulh3Requirements /h3ulliPhD (preferred) or MSc in Statistics, Biostatistics, or a related discipline, with strong experience in the pharmaceutical industry /liliStrong experience in at least one phase of clinical development, with at minimum exposure to late stage or regulatory facing activities /liliAbility to design, analyse, and interpret clinical trials and communicate statistical concepts clearly to non‑statisticians /liliExperience working in cross‑functional, international project teams /liliWorking knowledge of statistical programming (e.g. SAS or R) and sample sizing tools (e.g. EAST, nQuery, WinBugs) /liliUnderstanding of CDISC standards and regulatory expectations (e.g. FDA/EMA) /li /ulh3About Us /h3pUCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9,000 people in all four corners of the globe, inspired by patients and driven by science. /ph3Why work with us? /h3pAt UCB, we don’t just complete tasks, we create value. We aren’t afraid to push forward, collaborate, and innovate to make our mark for patients. We have a caring, supportive culture where everyone feels included, respected, and has equal opportunities to do their best work. We “go beyond” to create value for our patients, and always with a human focus, whether that’s on our patients, our employees, or our planet. Working for us, you will discover a place where you can grow, and have the freedom to carve your own career path to achieve your full potential. /ppAt UCB, we’ve embraced a hybrid-first approach to work, bringing teams together in local hubs to foster collaborative curiosity. Unless expressly stated in the description or precluded by the nature of the position, roles are hybrid with 40% of your time spent in the office. /ppUCB is an equal opportunity employer. All employment decisions will be made without regard to any characteristic protected by applicable laws. /ppShould you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on Please note should your enquiry not relate to adjustments; we will not be able to support you through this channel. /p /p #J-18808-Ljbffr