Senior Clinical SAS Analyst/Programmer, MS., a degree in Pharmacy, Regulatory Affairs., with 2 years of experience, Work on clinical trials data ranging from phase I/II/III for different therapeutic areas. Create datasets, tables, listings & figures for different submissions using SAS Enterprise guide 7.1, Universal Viewer & 9.2/9.4 soft. Create SDTM & ADaM SAS datasets for different studies & validate them by double programming. Use various SAS/STAT proc.(Proc Anova, Glm, Logistic, Lifetest) to create outputs for different analysis. Generate ISS, ISE analysis datasets, tables for multiple clinical trials with usage of SAS/Base & Sas/Sql. Create/Modify macros to facilitate reporting using SAS/Macro facility. Generate summary reports for internal analysis (UPAs using Sas/Ods & Sas/Graph). Use Medical Coding Dictionaries like MedDRA & WHO Drug to create datasets & outputs for NDA submissions. Work on validation reports using Pinnacle 21 Community Validator.
Must be willing to travel and/or relocate to work in unanticipated locations throughout the US.
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