Naresh Siliveri

• Around 9 years of experience as a SAS Programmer in Clinical Domain and has good exposure in different phases of clinical trials. • Good experience in all phases (Phase I to IV) of clinical trials: analyzing clinical data, creating tables, listing and generating reports. • Adequate knowledge on CDISC Standards (SDTM and ADaM). • Experience with Data Validation, designing Edit check programs and parallel development of tables & listings for project level programs.

~ Creating and reviewing programming specification document ~ Creating SDTM & ADaM datasets, tables and listings ~ Validating and transforming datasets as per client assignment specifications ~ Validating SAS programs as per client assignment specifications ~ Involved in SDTM creation and spec preparation using raw data, protocol and CRF ~ Understanding client specific macros ~ Worked as Point of Contact for couple of studies.

~ Reading and understanding the program specifications document ~ Validating and transforming datasets as per client assignment specifications ~ Validating SAS programs as per client assignment specifications ~ Developing automation programs for internal and external customers ~ Involved in SDTM creation and spec preparation using raw data, protocol and CRF.

~ Drug Discovery Des & Development ~ Green Biotechnology ~ Biosensors & Analytical Technique

~ Genetics ~ Biostatistics ~ Molecular Biology ~ Immunology ~ Bioinformatics ~ Bio Ethics