Writing SAS programs from instructions provided by Biostatisticians and Statistical Programmers to create CDISC data sets, tables, figures, and listings reporting and submitting the results of clinical trials for investigational medications Utilize SAS language, procedures, and options commonly used in clinical trial reporting including the Macro language, BASE SAS, SAS/STAT and SAS/GRAPH Create all files, documents, and analyses necessary to support an electronic submissions in eCTD format, including ISS/Client Work with all types of safety data and coding dictionaries (MedDRA and WHODRL) commonly used by the pharmaceutical industry
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