Key Duties and Responsibilities : Displays basic familiarity with many of the SAS procedures and options commonly used in clinical trial reporting including the Macro language, BASE SAS, SAS/STAT and SAS/GRAPH Codes SAS programs for applications designed to analyze and report clinical trial data and for electronic submissions of data in CDlSC format with instruction or input from supervisor Performs quality control checks of SAS code….
Key Responsibilities : Minimum of 4 years experience with SAS ideally in a clinical research environment ideally with knowledge producing outputs as well as datasets Minimum 2 years of R / R Shiny with standard packages for data visualization and analysis in aid of clinical data review in the Pharmaceutical & Biotech industry.
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