Good programming experience with various SAS functions, SAS procedures like PROC SORT, PROC PRINT, PROC MEANS, PROC CONTENTS, PROC FREQ, PROC FORMAT, PROC TRANSPOSE, PROC REPORT, PROC COMPARE, PROC IMPORT, Data set options and system Options, Data Manipulation techniques and statistical techniques. Having experience on programming techniques like reading external data files, merging the data, managing data, cleaning data, creating different outputs using SAS/ODS Expertise in analyzing clinical trial data, generating reports, tables, listings using SAS in accordance with the Statistical Analysis Plan (SAP), Standard Operating Procedures (SOPs) and departmental guidelines. Having a good working experience on creating and validating Analysis datasets and SDTM datasets. Good working experience on different types of Clinical trial data like Demographic data, Adverse Events, Laboratory data, Vital Signs etc. Experience in extracting, manipulating data, and creating Data Sets from various external sources like Excel, flat files using different techniques. Extensive familiarity with CDISC-SDTM standards, Domains, SDTM Implementation Guide (3.1), and CDISC- ADaM standards.
