• Over six years of experience in SAS, developing and implementing various applications in the pharmaceutical and clinical industries.
• In-depth knowledge of statistical analysis techniques for clinical and pre-clinical studies, and excellent experience in analyzing safety and efficacy data for Phases (I-III) clinical trials.
• Excellent knowledge of statistical procedures: PROC REPORT, PROC SUMMARY, PROC EXPORT, PROC ANOVA, TTEST, PROC MEANS, PROC UNIVARIATE, PROC REG, PROC CORR, PROC FREQ, PROC TRANSPOSE,GPLOT, and GCHART.
• Generate reports, tables, listings, and graphs according to Statistical Analysis Plan, Standard Operating Procedures (SOPs) and departmental guidelines. Generated reports using PROC REPORT and DATA _NULL_ for customized report writing.
• Expertise in storing and managing data in SAS files, merging SAS data sets, using MACROS, SAS procedures (PROCs), PROC SQLs, SAS Formats, and SAS Informats.
• Experience in data transformations & edit check an<