Over 3 years of experience in programming clinical trial data by using SAS 9.X versions.Hands on Experience in using SASSTAT, /BASE, SAS/SQL, SAS/ MS-EXCEL. Responsible for Developing reports for Safety and efficacy as per study requirements. Worked closely with the Statisticians, Data managers to provide SAS programming insights in analyzing Clinical Trial Data, generating final reports, tables and listings. Extensive use of SAS procedures like Proc Report, Proc Print, Proc Means, Proc Freq, Proc Sort, Proc Transpose, Proc Import, and Proc Export for data manipulation and analysis. Generated output files in RTF, HTML, and PDF format using SAS/ODS.Involved in Phases I to IV of the Clinical Trials in different therapeutics areas. Proficient in understanding of Study Protocols, SAP (Statistical analysis plan) and CRF’s. Having Knowledge of CDISC-SDTM, MedDRA and WHODD for Regulatory submission, ICH GCP Guidelines.