SAS programmer with good experience in SAS programming. Largely self-directed, confident, able to work both independently and as a team member. Highly productive and competent with good written and oral communication skills. Good with Intellectual ability to identify and analyze the problem, technical and scientific knowledge to solve problems. Experience in working on multiple protocols and/or drug compounds at a time, ability to create SDTM and ADaM datasets using CDISC and FDA guidance, create specified structure of TLFs through creating Macros and macro variables, perform extensive QC (Quality Check) and analysis in reviewing other team members work as well as render primary support and assistance in data validation and data cleaning in all phases of Clinical studies.