The position requires a Masters degree, or foreign equivalent, in Biostatistics, Chemistry, Scientific Discipline, or a related field plus two 2 years of experience in the job offered or a related occupation. Position also requires demonstrable experience with each of the following Demonstrable experience writing SAS programs to create data sets, tables, figures, and listings reporting results of clinical trials for investigational medications; Demonstrable experience with creating all files, documents, and analyses necessary to support an electronic submissions in eCTD format; Demonstrable experience with all SAS language, procedures, and options commonly used in clinical trial reporting including the Macro language, BASE SAS, SASSTAT and SASGRAPH; Demonstrable experience with the CDISC SDTM and ADaM models and transforming raw data into these standards; and Demonstrable skills at performing quality control checks of SAS code and output produced by other Statistical Programmers. Telecommuting permitted up to 100
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