CSL in Opfikon, Switzerland is seeking a Senior Statistical Programmer responsible for the design and implementation of SAS programs for analyzing clinical trial data. The role involves collaboration with study teams to ensure the submission readiness of clinical data and leading various statistical analyses.
Candidates should have a BSc in a relevant field and at least 5 years of experience in clinical programming, preferably in a CRO environment. Strong communication skills and fluency in English are required.
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