Description
SUMMARY OF QUALIFICATIONS * Certified SAS/Statistical programmer with over 7 years of experience in data analysis and statistical programming in phases I-IV of clinical trials working for Pharmaceutical companies and CROs in various therapeutic areas with high proficiency and within given timeline * 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 * Designs, develops and validates SDTM mapping specifications and ADAM specifications, data definition files and annotated case report forms * Experience in designing and developing Metadata and SAS programming for generating Define.xml * Experience in extracting, manipulating data, and creating Data Sets from various sources like Excel, flat files, Oracle database, Access database using PROC IMPORT techniques and SQL pass through facility * Generate reports using PROC REPORT for customized report writing * Expertise in producing RTF, PDF files using SAS ODS facility * Highly motivated individual with excellent organizational and interpersonal skills. Strong experience on Base SAS, SAS/Stat, SAS/Access, SAS/Graphs and SAS/Macros, SAS/ODS and SAS/SQL in Windows and Unix Environment * Strong knowledge involving all phases (I-IV) of clinical trials and statistical modeling techniques (linear, nonlinear, longitudinal analysis, survival analysis) * Excellent ability in problem solving, data analysis, complex reports generation
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