We are looking for a Data Management Programmer who is passionate, detail-oriented, and proactive to join us in our Global Clinical Sciences and Operations team, based in our Brussels office in Belgium or Monheim, Germany.

About the role

As a DM Programmer, you will play a pivotal role in shaping how clinical data is collected, structured, and delivered. You’ll lead programming activities across the data lifecycle—from building Case Report Forms (CRFs) using cutting-edge tools, to managing SDTM (Study Data Tabulation Model) deliveries with precision.

Who you’ll work with

You will collaborate with representatives from clinical, statistics, and CRO partners to finalize the design, creation, and implementation of Electronic Data Capture (EDC) solutions. You will also work closely with the Asset Data Lead/Study Data Lead to provide regular updates on progress for assigned studies.

What you’ll do

• Translate protocols into data collection requirements using the standards library to create study-level eCRF specifications.
• Lead the eCRF design process and manage study timelines related to data collection build and SDTM activities.
• Specify and oversee third-party data transfers and SDTM conversion requirements.
• Drive the end-to-end SDTM delivery process, ensuring quality and compliance.
• Champion the use and re-use of data standards at the study team level.
• Support submissions, audits, and inspections as required.

Interested? For this role we’re looking for the following education, experience, and skills

• Bachelor's Degree in a relevant field; advanced degrees preferred.
• At least 5 years of relevant experience in database design in a clinical or pharmaceutical-related field.
• Proficiency in eCRF design and experience with Data Management processes, including SDTM standards requirements.
• Strong analytical skills with the ability to apply critical thinking to translate protocol requirements into data collection tools.
• Advanced written and verbal communication skills with proficiency in English and the ability to work cross-culturally.
• Experience in managing aggressive deadlines and working on concurrent studies.

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 around 8,500 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.

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.