Biostatistician - Antwerp


We are currently in need for an Principal Biostatistician to form their Biometrics group. The basis for high quality results lies with the design of our clinical development plans and the studies they consist of. Based on your extensive experience you will act as the go-to-expert within our project teams and study teams when it comes to determining the most appropriate statistical study designs from statistical perspective.


Together with their clinicians and other study team members you will be challenged on a daily basis in your search for the most optimal design and methodology for analysis for every single study, while staying within the borders of the regulatory guidelines. For this reason there will be a high focus on practical experience but at the same time keeping your knowledge up to date. Furthermore, you will be interacting with CRO statisticians to ensure the highest quality of the performed statistical analyses and deliverables of your studies. In short you will be:

  • Acting as functional expert in clinical project sub teams
  • Participating in the clinical study protocol writing of new phase I-II-III clinical studies (design, sample size, assessments and statistical methodology) and be involved in the setup of the data capture tools
  • Interfacing with the CRO statisticians to discuss statistical data analysis, write the SAP, perform a thorough QC of the derived data and TLFs provided by the CRO, and provide input in the study reporting
  • Take ownership of the database and interface with the CRO on database management


What are we looking for?

  • Master or a PhD in sciences (e.g. biomedical sciences, mathematics, biology with an additional Master in (Bio)Statistics
  • 8 years of experience in clinical drug development.
  • You enjoy to work in cross-functional teams and would like to be a part of a newly formed group of people


If interested in this expert Biostatistician position please get in touch with Jord Teeuwen +31(0)23-7548660



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