Principal Statistician

Make your mark for patients

We are looking for a Principal Statistician to join us in our Biometrics & Data Science team to be based in any of our Brussels (Belgium) Monheim (Germany) Slough (UK) or Raleigh (US) offices.

About the role

You will be supporting latestage 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.

You 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 highquality outputs and ensure our trials are decisionready regulatorready and inspectionready.

Who youll work with

You will report to a Project Lead Statistician and work within a highly collaborative international Biometrics & Data Science team embedded in global development programs.

What youll do

• Provide statistical leadership for one or more indications or compounds with a focus on Phase 2/3 and latestage development
• Act as a trusted biometrics partner within crossfunctional program teams influencing development and regulatory strategy
• Take accountability for highquality statistical deliverables including study design input DMC activities analyses and regulatoryfacing outputs
• Translate development objectives into robust practical and innovative quantitative solutions.
• Work closely with the Project Lead Statistician Clinicians Programmers and Regulatory colleagues to enable timely informed decisionmaking
• Identify risks and opportunities early contributing thoughtfully to solutions

Interested For this position youll need the following education experience and skills:

• PhD (preferred) or MSc in Statistics Biostatistics or a related discipline with strong experience in the pharmaceutical industry
• Strong experience in at least one phase of clinical development with at minimum exposure to late stage or regulatory facing activities
• Ability to design analyse and interpret clinical trials and communicate statistical concepts clearly to nonstatisticians
• Experience working in crossfunctional international project teams
• Working knowledge of statistical programming (e.g. SAS or R) and sample sizing tools (e.g. EAST nQuery WinBugs)
• Understanding of CDISC standards and regulatory expectations (e.g. FDA/EMA)

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!

About us
UCB 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.

Why work with us
At UCB we dont just complete tasks we create value. We arent 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 thats 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.

At UCB weve 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.

UCB is an equal opportunity employer. All employment decisions will be made without regard to any characteristic protected by applicable laws.

Should 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.