Clinical SAS Programmer Resume Chicago - Hire IT People

TECHNICAL SKILLS

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 .