Clinical SAS Programmer – CDISC/Trials

A global pharmaceutical company in Milan is seeking a Statistical Programmer to support the programming of outputs for clinical studies. This role requires a scientific degree and 3-5 years of experience in a CRO or pharmaceutical company. The ideal candidate is proficient in SAS and has a clear understanding of CDISC standards. You will be responsible for programming and validating outputs, as well as supervising dataset generation. This opportunity offers a collaborative work environment and a full-time contract.
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