Ref: MEC 235
The Statistical Programmer acts as a functional expert in the field of SAS-programming and CDISC data standards and is foreseen as an active stakeholder that contributes to departmental strategic initiatives.
In particular, you will be:
The successful candidate has a BSc or preferably MSc in (biomedical) sciences, including a statistical part of curriculum, with at least six years of strong SAS-Programming experience in life science/pharmaceutical environment (and/or relevant experience within CRO).
He/She shows proficiency with Base SAS, SAS macro language, various SAS procedures and SAS GRAPH, preferably accompanied with SAS Institute certificate(s) such as “Base Programmer”, "Advanced Programmer" and/or “Clinical Trials Programmer”.
Furthermore she/he has in-depth working knowledge and understanding of CDISC SDTM and ADaM data standards, as well as understanding of basic statistics, data management concepts and clinical trial data. He/She should be able to organize and plan multiple priorities, and have the ability to collaborate with and coordinate External Service Providers. Last but not least, having excellent interpersonal and communication skills is required, together with being fluent in English (oral and in writing).