Senior Principal Programmer, Raleigh, NC
HybridMettmann, North Rhine-Westphalia, Germany
Job Summary
Review and coordinate clinical trial analysis and reporting setup requests to ensure accuracy and timely delivery. Configure study structures, repositories, and datasets in line with CDISC and governance requirements. Manage role-based access and Git/Azure DevOps resources while coordinating environment provisioning with platform administrators. Support programming teams during onboarding, legacy system transitions, and daily operations as a first-line technical contact. Improve lifecycle management by documenting processes, supporting validation activities, and automating practical solutions. This role joins the Programming, Visualization and Reporting team at UCB, a global biopharmaceutical company focused on neurology and immunology. The position requires a hybrid schedule with 40% office time.
Required Qualifications
- 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 experience with Tables, Figures, and Listings
- experience in regulated pharmaceutical environments with understanding of 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
- hybrid work arrangement with 40% of time spent in the office
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