Senior Principal Programmer (UK)

Make your mark for patients

We are looking for a Senior Principal Programmer (Statistical Computing Environment Business Coordinator) who is collaborative detail-oriented and compliance-minded to join our Programming Visualization and Reporting team based in any of our Brussels (Belgium) Monheim (Germany) Raleigh (USA) or Slough (UK) offices.

About the role

You will help clinical programming teams move to and work confidently within UCBs modern Statistical Computing Environment. You will translate clinical reporting needs into well-governed study setups support compliant platform operations and help improve the way teams generate validate and deliver clinical trial analysis and reporting outputs.

Who youll work with

You will work with the Programming Visualization and Reporting team statistical programming teams platform administrators Biometrics partners and business stakeholders. You will connect technical and business needs support users through onboarding and daily operations and help teams follow consistent compliant and practical ways of working.

What youll do

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 youll 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.

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.