Experience – Clinical SAS Programmer with over nine years (9) of experience in Pharmaceutical industry, with strong background in Clinical Trials, end-to-end Clinical Study Reporting, CDISC Data Standard, and SAS programming Expertise – Adept in statistical modeling and clinical statistical programming, especially in the areas of SAS Programming and SAS Drug Development for different health authorities. Strong programming experience gained from development of CDISC (SDTM, define.xml, ADAM) database, and end-to-end clinical reporting Industry Standards – Deep knowledge of Clinical Trials, Pharma R&D Value Chain, Investigator Collaboration Portal, Investigator Initiated Trials, SDTM and CDSIC standards Projects – Provided leadership to new drug development projects in liaison with biometricians and statistical scientific counterparts across the globe (Asia-Pacific, Europe and United States)