Temp SAS Programmer

Position Responsibilities: - Writing SAS programs 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 - CDISC SDTM and AdaM models and transforming raw data into these standards - Create all files, documents, and analyses necessary to support an electronic submissions in eCTD format, including ISS/ISE - Work in a team environment providing technical leadership and solving clinical trial reporting problems of moderate to high complexity within budget and customary time line constraints while assuring high quality standards - Perform quality control checks of SAS code and outputs -Thereputic areas include, but are not limitted too; Oncology, Immunology, CNS, Inflamation, and Pain Position Qualifications: Minimum Qualifications: - Bachelor's degree in Biostatistics, Statistics, Computer Science, or a related field; with years of SAS and pharmaceutical industry experience - CDISC SDTM and AdaM expertise

To find out more about Real please visit www.realstaffing.com [1]

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[1] http://www.realstaffing.com