An exciting long term contract opportunity for a SAS programmer has become available with a large pharmaceutical client based in Cambridge MA. Job Description 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 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 with all types of safety data and coding dictionaries (MedDRA and WHODRL) commonly used by the pharmaceutical industry 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 output produced by other Statistical Programmers Essential Skills 4+ years SAS programming experience Strong applicable CDISC experience including the conversion of raw data sets Strong Clincal Background Bachelors Degree in related subject MUST BE ABLE TO WORK ON SITE IN CAMBRIDGE MA. (Real Staffing Group acts as an Employment Agency and an Employment Business)