At a Glance
- Tasks: Lead programming teams in clinical trial analysis and reporting with innovative tech.
- Company: Join UCB, a global biopharmaceutical company focused on neurology and immunology.
- Benefits: Enjoy a supportive culture, hybrid work, and opportunities for career growth.
- Other info: Collaborative environment with a focus on innovation and patient value.
- Why this job: Make a real impact on patient outcomes while working with cutting-edge statistical tools.
- Qualifications: 5+ years in clinical trials, strong knowledge of CDISC standards, and programming experience.
The predicted salary is between 63000 - 77000 £ per year.
Operations, and help teams follow consistent, compliant, and practical ways of working. You will review and coordinate clinical trial analysis and reporting setup requests, making sure they are complete, accurate, and delivered on time. You will configure study structures, repositories, datasets, reporting components, and access in line with CDISC and governance requirements. You will manage role-based access, study configurations, and Git/Azure DevOps resources using approved requests and compliant processes. You will coordinate environment provisioning with platform administrators so study teams can begin work in a ready and reliable environment. You will support programming teams during onboarding, transition from legacy systems, and ongoing operations as a first-line technical contact. You will improve lifecycle management and workflows by documenting processes, supporting validation activities, and automating practical solutions that enhance quality and user experience.
Interested? For this position you'll need the following education, experience and skills:
- You bring 5+ years of experience in clinical trial results generation, reporting, and submission processes.
- You have experience supporting Statistical Computing Environments, including process flows, user access, and Biometrics requirements.
- You understand CDISC standards, including SDTM and ADaM, and have worked with Tables, Figures, and Listings.
- You have worked in regulated pharmaceutical environments and understand SDLC, validation, audit readiness, and compliant configuration expectations.
- You can communicate clearly with technical teams and business stakeholders, while tracking setup processes across systems and teams.
- You bring practical experience with tools such as Domino Data Lab, SAS, R, Git, Azure DevOps, VS Code, or SAS Studio.
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 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. At UCB, we've embraced a hybrid-first approach to work, bringing teams together in local hubs to foster collaborative curiosity.
Senior Principal Programmer (UK) in Princes Risborough employer: UCB S.A.
UCB is an exceptional employer that prioritises innovation and collaboration, making a significant impact in the biopharmaceutical industry. With a supportive work culture that values inclusivity and personal growth, employees are encouraged to explore their potential while contributing to meaningful patient solutions. Located in Slough, UK, UCB offers a hybrid-first work environment, allowing for flexibility and teamwork, ensuring that every team member can thrive both professionally and personally.
