• Statistical Programmer with nearly 8 years of SAS programming experience in Pharmaceutical and Contract Research Organizations with emphasis on analysis, development, validation and implementation of various projects. • Working knowledge on different phases of Clinical Trials (Phase I – III). • Creating SDTM,ADaM datasets and their validation, Open CDISC Validator, EDC • Mapping Specifications, standardize the data values using CDISC Controlled Terminology(MeDRA aFnd WHO), Define.xls • Extensively involved in Clinical Data Analysis and preparation of SAS Datasets, reports, tables, listings, summaries and graphs according to the Standard Operating Procedures (SOPs) and departmental guidelines. • Extensive knowledge in SAS tools like SAS/Base, SAS/SQL, SAS/Macros, SAS/Graphs, SAS/Stat and SAS/ODS. Knowledge on Data ware house concepts. • Experienced in importing and exporting Data from SAS, • Knowledge on Hadoop and Core Java sevlets jdbc jsp frameworks like struts,springs and Hadoop • Good knowledge on SAS Visual Analytics • Created and maintained SAS macros and utilities. • Good knowledge of CDISC Standards • Extensive experience in data analysis and reporting. • Experienced with good knowledge on clinical trial phases, clinical protocols, CRF’s/Annotated CRF’s, ICH, FDA Regulation and GCP guidelines. • Proficient in handling multiple projects. • Excellent analytical and problem solving skills. • Experienced in independently and effectively organizing and managing multiple assignments with