• Contract
  • Remote



  •  Strong SAS programming skills required, with proficiency in SAS/Base, SAS/Stat, and SAS Macros 
  • Generate analysis datasets, tables, figures, and listings to support the statistical analysis of clinical trials data
  • Generating SDTM domains, ADaM datasets
  • Providing programming input to CRF, SAP, analysis file specifications, and tables, figures, and listings (TFLs) shells;
  • Writing SAS programs to generate derived analysis datasets, perform analysis, and TFLs
  • Performing programming validation to ensure the quality of analysis datasets and programming outputs; ensuring consistency and adherence to standards within the project;
  • Providing programming support for the preparation of integrated reports, submissions and post-submission activities;
  • Converting, verifying and integrating multiple sources of incoming data for the creation of analysis datasets; serving as a coordinator when multiple programming resources (e.g. CROs or contractors) are used
  • Contributing to the creation, maintenance, and validation of standards for outputs and macros.


  • Bachelor’s degree in computer science, statistics, mathematics, life sciences or other relevant degree.
  • 7 years of statistical programming experience in the pharmaceutical/biotechnology industry.
  • Early Development experience preferred
  • Strong understanding of CDISC standards, including SDTM and ADaM models and experienced in implementing these models
  • In-depth knowledge of FDA/ICH guidelines and industry/technology standard practices.
  • Demonstrated proficiency in using SAS to produce derived analysis datasets and produce tables, figures, listings, (TFLs) and graphs (required for adhoc analysis).
  • Experience working with raw data (Rave) and overall knowledge of Rave database/data structure. 
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