Over 30+ years experience in Software Development, involving in Design, Analysis, and implementation. Extracted, Prepared and Validated data for Clinical trial Phases II, III and IV. Knowledge of FDA regulated Clinical trials and drug approvals. Hands on experience in interfacing SAS with RDBMS like Oracle 8X, Oracle Clinical and reading raw data from within various file formats. Developed SAS Macro Library of development and production level Utility Macros used for performing and reporting statistical analysis. Experience in both Safety and Efficacy data Analysis and Reporting. Taught IT classes at local colleges and university. Well versed with the latest developments in information technology. Professional image and excellent communication skills.