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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 UCB’s 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 you’ll 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 you’ll do
- Review and coordinate clinical trial analysis and reporting setup requests, making sure they are complete, accurate, and delivered on time.
- Configure study structures, repositories, datasets, reporting components, and access in line with CDISC and governance requirements.
- Manage role-based access, study configurations, and Git/Azure DevOps resources using approved requests and compliant processes.
- Coordinate environment provisioning with platform administrators so study teams can begin work in a ready and reliable environment.
- Support programming teams during onboarding, transition from legacy systems, and ongoing operations as a first-line technical contact.
- Improve lifecycle management and workflows by documenting processes, supporting validation activities, and automating practical solutions that enhance quality and user experience.
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Interested?
For this position you’ll need the following education, experience and skills:
- 5+ years of experience in clinical trial results generation, reporting, and submission processes.
- Experience supporting Statistical Computing Environments, including process flows, user access, and Biometrics requirements.
- Understanding of CDISC standards, including SDTM and ADaM, and have worked with Tables, Figures, and Listings.
- Experience in regulated pharmaceutical environments and understanding SDLC, validation, audit readiness, and compliant configuration expectations.
- Ability to communicate clearly with technical teams and business stakeholders, while tracking setup processes across systems and teams.
- Practical experience with tools such as Domino Data Lab, SAS, R, Git, Azure DevOps, VS Code, or SAS Studio.
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Internal applicants should be in their current job for at least 12 months, must meet performance standards and are not on formal corrective/disciplinary process (PIP), warning, final warning, or compliance warning letters within the last 12 months. Please inform your Manager or your Talent Partner before applying to any internal job opportunities.
At 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, this role is hybrid with 40% of your time spent in the office, irrespective of your current contractual agreement. Should your current working arrangements differ, please contact your Talent Partner to discuss, before submitting your application.
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 EMEA-Reasonable_Accommodation@ucb.com. Please note should your enquiry not relate to adjustments; we will not be able to support you through this channel.
Requisition ID: 93689
Recruiter: Kevin Ross
Hiring Manager: Tim Williams
Talent Partner: Natacha Tassier
Job Level: MM I
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