Sruthi G
********.*****@*****.***
SUMMARY:
Certified SAS Programmer with Seven years of experience in working with SAS and SAS
tools emphasizing on analysis, design, development, testing and implementation of various
projects for Pharmaceutical and Biotechnology Industries on Windows and Unix
environment.
Extensive Experience in SAS/BASE, SAS/STAT, SAS/SQL, SAS/MACRO, SAS/GRAPH,
SAS/ACCESS, SAS/ODS, SAS/ENTERPRISE GUIDE and SAS/INSIGHT.
Experience in developing SAS procedures, macros, and applications for data cleaning,
programming, reporting, and documentation.
Worked with biostatisticians to provide SAS programming for analyzing the clinical trial data and
generating reports, tables, listings, and graphs.
Have extensive experience with SAS Programming, Oracle Clinical, Clinical Trials,
Reporting Tools, Oracle, PL/SQL and UNIX.
Extensive programming experience with proc SQL, proc report, proc tabulate, proc transpose,
proc gplot, proc gchart, proc datasets, proc format, proc compare, proc append, proc import, proc
export, proc printto, proc transpose, proc print, SAS/STAT procedures such as proc corr, proc reg,
proc GLM, proc cluster, proc ANOVA, proc logistic, proc freq, proc means, proc univariate etc.
Extensive experience with concatenating, interleaving, and merging SAS datasets.
Worked on oncology and oncology related data.
Extensive experience in CDISC SDTM with MedDra dictionary coding/decoding skills
and also authorizing the mapping specifications from source data to CDISC SDTM and
sponsor defined Standards and also Quality Control of CDISC SDTM output.
Generated Tabular reports for Integrated Summaries of Safety (ISS) and Integrated Summaries of
Efficacy (ISE) for FDA regulatory submissions.
Involved in Documenting and reporting program validation inspections in compliance with 21
Code of Federal Regulations (21CFR, Part 11).
EDUCATIONAL QUALIFICATIONS:
Master of Science in Chemistry, Long Island University, New york.
Bachelor of Pharmacy, Kakatiya University, India.