• 10 years of experience in SAS programming of statistical reports, clinical database and statistical analysis for clinical trials • Have led a team of 2-3 people and worked as a POC • Experienced in the CDISC standard and the development of SDTM and ADAM datasets • Working with Statisticians in analyzing the Clinical Trial Data, generated reports, tables, listings and graphs using SAS in accordance with the Statistical Analysis Plan (SAP), Standard Operating Procedures (SOPs). • Experience in developing, validating and implementing SAS programs and produce derived datasets for analysis and generating & documenting tables, listings and graphs for clinical study reports. • Worked on CRF annotation, Creating define.xml, submission ready packages • Excellent knowledge of SAS Procedures: PROC FREQ, PROC UNIVARIATE • Generated reports using PROC REPORT, PROC TABULATE for customized report writing. • Experience in producing RTF, HTML files using SAS ODS. • Ability to manage multiple assignments and handle changing priorities in a fast-paced environment • Working on efficacy tables and graphs – writing macros for creating many outputs from single program • Experience in BASE SAS, SAS MACROS. • Certified Base SAS Programmer