Make your mark for patients

We are looking for a Data Management Programmer who is analytical, collaborative, and proactive to join our team in Global Clinical Sciences and Operations, based in our HQ in Brussels (Belgium).

About the role

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...