Data Management Programmer

You will turn clinical study protocols into practical data collection tools that teams can use with confidence. You will create and maintain electronic case report form (eCRF) specifications, external data transfer specifications, and study data documents. You will help studies start well, stay on track, and produce reliable clinical data.

Who you will work with

You will work with colleagues in clinical, statistics, and data management, as well as CRO partners and external data vendors. You are going to partner with study data leads and asset data leads to shape data collection, solve issues early, and support smooth study delivery across global teams.

What you will do

• You will translate study protocols into clear data collection requirements, including eCRF forms, instructions, checks, terminology, and alerts.
• You will create and maintain specifications for data received from external sources such as laboratories, eCOA providers, biomarker partners, and other vendors.
• You will lead eCRF design discussions with cross-functional teams and partners to support simple, consistent, and compliant EDC solutions.
• You will manage study timelines for data collection build and SDTM work, and you will raise risks early when plans may slip.
• You will review and validate data collection tools and support study documentation linked to SDTM mapping, datasets, and submission readiness.
• You will share your expertise in study data collection and support audits, inspections, and submissions when needed.

Do you have experience in Database design?, Do you have a Bachelor's degree?, * You will bring a bachelor's degree or equivalent experience in a relevant scientific, clinical, data, or technical field.

• You will have at least 5 years of experience in database design in a clinical, biotech, or pharmaceutical setting.
• You will bring hands-on experience with data management processes, eCRF creation, EDC systems, and technical specifications.
• You will have working knowledge of SDTM requirements and experience reviewing issues, logs, errors, and warnings.
• You will communicate clearly in English and explain technical topics in a way that is easy for non-technical colleagues to understand.
• You will be comfortable handling changing priorities, solving complex problems, and working independently while building strong partnerships.

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!

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. 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 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.   You must create an Indeed account before continuing to the company website to apply