Sr. Clinical Sas Programmer
Current• Worked extensively to generate SAS data sets, statistical reports, monthly reports, listings, and safety reports for cross-functional teams for Phase II to III of Cardio-Vascular Clinical Trial Data.• Created CDISC SDTM Domains Specification and Data Definition (define.xml) Documents.• Extensively worked on Data mapping from Existing Raw data to CDISC SDTM Standard, data mapping from SDTM to ADaM Domains, and review CRFs (Case Report Forms) to ensure consistency with protocol and adequacy in collecting data to meet objectives defined in the protocol.• Worked with the Statisticians, Data managers to provide SAS programming in analyzing Clinical Trial Data, and generating final study reports, tables, listings, and graphs.• Created edit check programs to find data discrepancies in raw datasets provided by Data Management Group.• Validated SDTM Analysis datasets, Tables, Listings and Figures.• Created SDTM datasets for safety and efficacy domains and Created SAS macros for SDTM mapping.• Generated tables, listings and graphs according to Protocol and Statistical Analysis Plan (SAP) using PROC MEANS,PROC FREQ,PROC TRANSPOSE, PROC REPORT, PROC GCHART and PROC GPLOT Procedures.• Created SAS Customized Reports using the Data _Null_ technique.• SAS/STAT procedures such as UNIVARIATE, FREQ, and MEANS were used to carry out analyses and the SAS REPORT procedure is generally used to display results.• Involved in creating all files, documents, and analyses necessary to support an electronic submissions in eCTD format• Used SAS ODS to produce HTML, PDF and RTF format files.• Involved in generating ISS (Integrated Summary of Safety) and ISE (Integrated Summary of Efficacy) analysis Datasets, Tables, Listing and Graphs for multiple trials.
