Job Overview: Writing SAS programs to create data sets, tables, figures, and listings reporting Utilizing SAS language, procedures, and options commonly used in clinical trial reporting including the Macro language, BASE SAS, SAS/STAT and SAS/GRAPH. Programming all aspects of a clinical trial, from files to tables and figures Using SAS in a quality control/ production capacity Write and edit programs to clean, manage, merge, and analyze data. Base SAS Certification and SAS advance certification is a plus. SAS clinical programmer with a minimum of 0-1 years of SAS clinical experience. CDISC, SDTM and ADaM.
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