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

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