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Sas Programmer Resume Profile

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CT

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Summary

  • About three years of experience in access, management, analysis, report and validation of clinical trial studies and Medicare data.
  • Proficient in data extraction, edit check, statistical analysis and report generation according to the Statistical analysis Plan SAP , Clinical Protocol, CDISC standards, and Electronic Submission standards using SAS/BASE, SAS/STAT, SAS/GRAPH, SAS/ACCESS, SAS/ODS, SAS/SQL, SAS/MACRO.
  • Experienced in descriptive statistics and inferential statistics using SAS/STAT.
  • QC and validation experience using PROC compare and openCDISC validator.
  • Experienced in generating RTF, HTML and PDF formatted files using SAS/ODS.
  • CDISC experience including SDTM, ADaM.
  • Good comprehension of FDA 21 CFR part 11 , CDISC Clinical Data Interchange Standard Consortium , Good Clinical Practices GCP , International Conference of Harmonization ICH E9 and other related regulatory guidelines.
  • One year of R D experience in design, synthesis and testing of potential tumor drug.
  • Worked closely with Biostatisticians and Data Managers in analyzing the Clinical Trial Data and generating Integrated Summaries of Efficacy ISE and Integrated Summaries of Safety ISS tables, listings and graphs for FDA submissions.

Skills:

SAS 9.1/9.2, SAS Tools such as SAS/BASE, SAS/STAT, SAS/GRAPH, SAS/ACCESS, SAS/SQL, SAS/ODS, SAS/MACRO, SDTM-CDISC 3.1.1/3.1.2, MS SQL Server, C/C , MatLab, Windows, Microsoft Office Word, Excel, PowerPoint and Access , MS Visio.

Projects Summary:

Confidential

Clinical SAS programmer

This position was to analyze the clinical trial data from phase I-IV

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