SUMMARY * About 26 years SAS and other system programming experience including 21 years full time programming experience for the pharmaceutical industry On time solution supplier in supplying, managing, and maintaining database design, deriving databases, programming, and statistical output used/created in support of clinical trials across indications Extensive experience in design, implementing, and validating of programming systems Extensive experience in large system development and data architecture with complex data management and data interface characteristics Strong management skill in team/effectiveness/stress less working Strong background of Computer Science, and Statistics Extensive experience in supporting electronic submission, ISS/ISE, publication and ad-hoc analyses for clinical trials in ADAM/SDTM standard Invented a clinical try programming process (with help of automation objective macros) so that, for most cases, two programmers can complete double programming works in two weeks for a Phase I study and in six weeks for a Phase II/III/IV study Programmers can be dynamically coordinated to a study in any stage of the study across therapeutic areas and regions. Managed programmers to support clinical studies in the middle of a study (especially for Phase II, III, IV) in a high quality with very short timeline Parallel studies, Ongoing Study Monitoring/Reporting, Study Integration, Ad hoc, AD Com, Patient profile/Site listing/Narrative/define.xml generation, and Publication requests can be handled quickly with much less efforts. * MS-WINDOW95, MS-NT, UNIX, and VAX/VMS. * SAS, SAS/IntrNet, C/C++, Perl, Shell, HTML, JavaScript, VISUAL BASIC, PL/SQL, Designer/2000, PRO*FORTRAN, COBOL, DECforms, TRUE change, Visual SourceSafe, and Visio. * ORACLE, SYBASE, SQL Server, and MS ACCESS. * Clinical Trial, Statistical Analyses, Object Oriented Design, Risk Management, and Process Modeling & Optimization.