Good knowledge in CDISC , SDTM ,ADaM Very good knowledge in Clinical Trials, Clinical Data Analysis, Clinical Data Integration and Standardization, Generating Statistical Analysis Files, Tables, Listings, Graphs, Validations, and Documentation. Import and Export to another data file formats, including Delimited files, DBF, MDB and Spreadsheet files. Expert in using SAS ODS to create HTML, RTF and PDF output files and Data _Null_ to generate ad hoc and customized reports. Generate Reports, Tables, Listings, Graphs and Summaries as per company standards and in compliance with 21 CFR Part 11, FDA Data Extraction, Transformation, and Loading (ETL) from disparate Data sources like Multiple Relational Databases like Oracle, SQL Server, and MS Access. Got good knowledge of SAS/EG, SAS/ETL, SAS/BASE, SAS/SQL, SAS/MACROS, SAS/GRAPH, SAS/ACCESS, SAS/ODS in Windows and UNIX environment. Thorough knowledge in complete GCP and ICH guidelines, SOP’s, and 21CFR Part 11. Develop SAS programs for various analyses in Phases I, II and III of Clinical Trials Able to perform different operations on SAS data sets of any size like Sorting, Concatenating, Merging, and Interleaving. Integrate data to process clinical trial studies from multiple sites for statistical evaluation. Producing external files and reports employing various SAS procedures, like Proc Print, Proc Report, Proc Summary, Proc Mean, Proc Transpose, Proc SQL, generating reports, tables, listings, and graphs using various procedures like proc SQL, proc means, proc univariate, proc freq, proc datasets, proc format, proc compare, proc append, proc gplot, and proc gchart.