Positions range from junior to senior levels. Responsible for editing and validating programs using SAS macros to generate listings and tables for the study reports and NDA submissions, data step manipulations for data quality assurance/validation of table, listing and summaries, using SAS to analyze clinical data from CRF's creating SAS data sets for the purpose of analysis and report writing for clinical trials (Pre-clinical through Phases IV), generating efficacy and safety reports, creating datasets and generating reports using PROC Tab, PROC Report, Data Null, SAS arrays, PROC SQL and Macros, and verify and document programs.

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