Extensive Pharmaceutical Industry SAS programming experience in the analysis and reporting of Phase II-IV clinical trial data, project and programming team management, client interaction and support.• Successfully led the SAS programming activities for six New Drug Applications to world- wide health authorities, with focus on Hepatitis C and Cardiovascular therapy areas.• Collaborated extensively with staff and senior management in Clinical, Statistical, Regulatory, Medical Writing and Data Management Departments to define programming requirements and discuss solutions to novel problems. • Led the technical development for several department level standards initiatives.• Developed SAS programs to produce clinical reporting databases, analysis datasets, summary tables, and SAS transport files.• Provided creative and innovative technical SAS solutions to unique business problems in clinical trial reporting.• Hands-on management style included setting technical standards and strategies, participating in project programming, and quality review of deliverables. Project management emphasized programming team interaction with shared as well as individual accountability for quality. • Trained, coached, and mentored others in corporate and educational settings.Specialties: SAS ProgrammingClinical Trial ProgrammingSAS MACROSSDTM, ADaMSQLProject ManagementProgramming Team ManagementClinical Research SupportUNIX, PC SASMainframe OS/JCL, TSO/ISPF, CLIST