Summary * Certified Base Programmer for SAS 9 with 5+ years of biostatistical programming experience in CRO, hospitals, pharmaceutical, and healthcare industries. * Involved in drug development process with experience in analyzing, reporting, and reviewing pre-clinical/clinical trial data. * Good understanding of FDA submission (IND, NDA) process, clinical protocols, CRFs, CDISC (SDTM, ADaM), 21 CFR Part 11, GCP, and IRB guidelines. * Experienced in developing, debugging, and validating project specific SAS programs to generate SAS derived datasets, summary tables, listings, and graphs of clinical and healthcare data. * Performed coding, testing, maintaining, and documenting new SAS programs and enhancing efficiency of existing programs using SAS/BASE, SAS/MACROS, SAS/SQL, SAS/STAT, SAS/GRAPH, SAS/ODS, SAS/ACCESS.

Highlights:

• SAS
• Proc
• Programming
• Statistical Analysis
• SAP
• Research
• Statistics
• Structured Query Language
• Management
• Test