SUMMARY * A Certified SAS Programmer with over six years of working experience in SAS applications for Clinical Research and Analysis. * Experienced working with Pharmaceutical companies and CROs. * In depth experience and knowledge in various SAS products such as BASE /SAS, SAS /MACROS, SAS/STAT, SAS/ACCESS, SAS/SQL in Windows and UNIX environments. * Worked extensively by using base/SAS, SAS/macro, SAS procedures (proc sort, proc sql, proc transpose) to output SDTM and ADAM datasets compliance with CDISC SDTM implementation guide 3.1.3 and ADAM ig v1.0. * Great knowledge and understanding of clinical trials study designs, study protocols, statistical analysis plans, (SAP), case report form (CRF/eCRF), annotated case report forms and company Standard Operating procedures (SOP). * Generated TLFs and reports(.rtf, .pdf) by using PROC report, ODS and SAS macros, PROC/STATS. * Experience and expertise in working for different therapeutic areas like Oncology, diabetic, neuroscience, autoimmune. * Worked for integrated summery of safety and efficacy datasets (ISS, ISE) at submission level. * Have great experience and knowledge of validation of datasets by using PROC FREQ, PROC COMPARE, PROC CONTENTS and by using parallel programming and pinacle21. * Possess strong ability to quickly adapt to new applications and platforms. * Experience in interacting with clients, multiple user groups and managing development teams.

Highlights:

Companies I like:

Mrs.

• Cancer
• Protocol
• SAP
• SAS
• Oncology
• PDF
• Proc
• Programming
• Statistical Analysis
• Structured Query Language