Senior Principal Programmer
Il y a 3 heures
Brussels, Belgique
UCB
Temps plein
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h3Make your mark for patients /h3 pWe are looking for a bSenior Principal Programmer /b (Statistical Computing Environment Business Coordinator) who is collaborative, detail-oriented, and compliance-minded to join our bProgramming, Visualization and Reporting /b team, based in any of our Brussels (Belgium), Monheim (Germany), Raleigh (USA), or Slough (UK) offices. /p h3About the role /h3 pYou 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. /p h3Who you’ll work with /h3 pYou 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. /p h3What you’ll do /h3 pYou will review and coordinate clinical trial analysis and reporting setup requests, making sure they are complete, accurate, and delivered on time. /p pYou will configure study structures, repositories, datasets, reporting components, and access in line with CDISC and governance requirements. /p pYou will manage role-based access, study configurations, and Git/Azure DevOps resources using approved requests and compliant processes. /p pYou will coordinate environment provisioning with platform administrators so study teams can begin work in a ready and reliable environment. /p pYou will support programming teams during onboarding, transition from legacy systems, and ongoing operations as a first-line technical contact. /p pYou will improve lifecycle management and workflows by documenting processes, supporting validation activities, and automating practical solutions that enhance quality and user experience. /p h3I nterested? For this position you’ll need the following education, experience and
skills:
/h3 pYou bring 5+ years of experience in clinical trial results generation, reporting, and submission processes. /p pYou have experience supporting Statistical Computing Environments, including process flows, user access, and Biometrics requirements. /p pYou understand CDISC standards, including SDTM and ADaM, and have worked with Tables, Figures, and Listings. /p pYou have worked in regulated pharmaceutical environments and understand SDLC, validation, audit readiness, and compliant configuration expectations. /p pYou can communicate clearly with technical teams and business stakeholders, while tracking setup processes across systems and teams. /p pYou bring practical experience with tools such as Domino Data Lab, SAS, R, Git, Azure DevOps, VS Code, or SAS Studio. /p pAre 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 /p h3About us /h3 pUCB 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. /p h3Why work with us? /h3 pAt 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. /p pAt 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 or precluded by the nature of the position, roles are hybrid with 40% of your time spent in the office. /p h3UCB is an equal opportunity employer. /h3 pAll employment decisions will be made without regard to any characteristic protected by applicable laws.br/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. /p
skills:
/h3 pYou bring 5+ years of experience in clinical trial results generation, reporting, and submission processes. /p pYou have experience supporting Statistical Computing Environments, including process flows, user access, and Biometrics requirements. /p pYou understand CDISC standards, including SDTM and ADaM, and have worked with Tables, Figures, and Listings. /p pYou have worked in regulated pharmaceutical environments and understand SDLC, validation, audit readiness, and compliant configuration expectations. /p pYou can communicate clearly with technical teams and business stakeholders, while tracking setup processes across systems and teams. /p pYou bring practical experience with tools such as Domino Data Lab, SAS, R, Git, Azure DevOps, VS Code, or SAS Studio. /p pAre 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 /p h3About us /h3 pUCB 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. /p h3Why work with us? /h3 pAt 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. /p pAt 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 or precluded by the nature of the position, roles are hybrid with 40% of your time spent in the office. /p h3UCB is an equal opportunity employer. /h3 pAll employment decisions will be made without regard to any characteristic protected by applicable laws.br/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. /p