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Clinical Sas Programmer Resume

ChicagO

TECHNICAL SKILLS

  • SAS/Base, SAS/Stat, SAS/Graph, SAS/Macro, SAS/SQL, SAS/ODS, SAS/Report.
  • Oracle Clinical, SQL Server, PL/SQL and MS Access.
  • MS Office Word, Excel, PowerPoint, Access and Outlook, SAS ODS.
  • SAS v 9.3/8.0.
  • UNIX, WINDOWS, MS - DOS.

PROFESSIONAL EXPERIENCE

Confidential, Chicago

Clinical SAS Programmer

Responsibilities:

  • Good knowledge on MedRA and WHO drug and controlled terminology.
  • Data standardization to teh SDTM domains as per teh 3.1.3 and 3.2 SDTM IG versions and specifications provided by teh client.
  • Developed teh ADaM datasets as per teh 1.0 ADaM IG version.
  • Write QC codes by implementing various statistical procedures like FREQ, MEANS, UNIVARIATE, SUMMARY, TRANSPOSE, SQL and PRINT.
  • Optimized performance using Data Validation and Data Cleaning .
  • Created CRT’s (Case Report Tabulations) and listing reports using Study Data Tabulation Model (SDTM) Model.

Confidential

SAS Analyst/Programmer

Responsibilities:

  • CRF annotation . Created CRT's (Case Report Tabulations) using CDISC standards.
  • Design and implement statistical reporting processes for regular data collection and clinical data analysis. Involved in analysis of Phase I, II and III Clinical Trials.
  • Created SAS Customized Reports using various reporting procedures for FDA submissions.
  • Produce tables and listings for Clinical Study Reports.
  • Develop routine SAS macros to create tables.
  • Performed statistical analysis, generated Ad hoc reports for Data Management .

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