Data Management Programmer at UCB
Monheim, , Germany -
Full Time


Start Date

Immediate

Expiry Date

19 Sep, 25

Salary

0.0

Posted On

20 Jun, 25

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Critical Thinking, Communication Skills, English, Database Design, Analytical Skills

Industry

Pharmaceuticals

Description

MAKE YOUR MARK FOR PATIENTS

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 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.

Responsibilities

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.

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!
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