Leading all biostatistics activities related to clinical trials as responsible project statistician; Development and review of statistical sections of protocols, including sample size calculations; Development of statistical analysis plans; Development and documentation of analysis database structures (i.e. SAS analysis dataset structures); Development of SAS program requirements and specifications; SAS programming and program validation
MSc in Statistics or equivalent; At least 5 years of industry experience in clinical research; At least 5 years of industry experience in biostatistics; At least 5 years of experience in SAS programming; Expert knowledge and understanding of the statistical principles, concepts, methods, and standards used in clinical research; Very Good knowledge and understanding of the SAS programming language
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