-SAS Programmer with nearly 4+ years of and Functional experience of exactly four years in clinical research and statistical analysis -Traveled across india for delivering trainings @ Mumbai, Banglore, Kolkata, Chennai, Kochi -Experience in Implementation, support and upgrade projects across the globe. -Handled all types of training at all levels including academic, corporate, certification, end-user, power users, and fresher -Training's were delivered to domestic and global clients including Vodafone,TCS,HP,IBM,Wipro,Deloitte,IGATE,Accenture,Novartis -Delivered training to Wipro kochi ,Chennai batches fresher and intermediate -Delivered training's for Accenture continuously for 5 batches @ Chennai, Bangalore and Pune -Delivered ILP training for TCS 2 fresher batches -Conducted workshop at Hyderabad for a Client Training -Good communication and Effective team leading capabilities -Easy to adopt and can provide training at any location. -Expertise in analyzing and coordinating clinical trial data, generating reports, tables, listings and graphs using SAS in accordance with the Statistical Analysis Plan(SAP),Standard Operating Procedures(SOPs) and departmental guidelines. -Strong knowledge involving all phases (I-IV) of clinical trials. -Trained in Good Clinical Practice (GCP), Regulatory Compliance and FDA Guidelines. -Strong experience on Base SAS, SAS/Stat, SAS/Access, SAS/Graphs and SAS/Macros, SAS/ODS and SAS/SQL in Windows Environment. -Optimized performance using Data Validation and Data cleansing on Clinical Trial data using Statistical procedures like PROC FREQ, PROC MEANS, and PROC UNIVARIATE. -Generate reports using PROC REPORT, DATA_NULL_ and PROC TABULATE for customized report writing. -Expertise in Data archival and Data migration, ad-hoc reporting and code utilizing SAS on UNIX and Windows Environments. -Expertise in producing RTF, PDF, HTML files using SAS