-An accomplished professional with more than 10 years of experience in healthcare industry
-Clinical SAS programmer with expertise in analyzing Clinical Trials and Post-Marketing Pharmacovigilance studies
-Generation of new data set by using PROC SORT, PROC APPEND, SET/MERGE functions, and DERIVING new VARIABLES
-Analyzing large data through PROC MEANS, UNIVARIATE, TTEST, ANOVA, GLM, NPAR1WAY, TRANSPOSE and PROC FREQ approaches
-Annotation, QC, Validation, Mapping, GAP analysis for raw/analyzed data for generation of CDISC -SDTM/ADaM data sets for FDA submission
-Generation of Integrated Summaries of Safety and Efficacy (ISS and ISE) data sets and reports
-Using Macros for Automation for...