Recordati is seeking a skilled Statistical Programmer to drive the programming of outputs (tables, listings, figures) and build SDTM/ADaM datasets for clinical studies. The role involves collaborating with statisticians, data managers, and safety teams to ensure CDISC-compliant deliverables and robust validation of programming utilities.
Ideal candidates have 3–5 years in CRO/pharma settings, strong SAS skills, and familiarity with CDISC and GCP guidelines.
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📌 Sas programmer - clinical trials data specialist (Milano)
🏢 Recordati
📍 Milano
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