* Certified SAS programmer with around seven years of experience in statistical programming with Emphasis on data management and statistical programming in various phases of clinical trials and SAS training.* Trained and placed 18 Batches of SAS programmers in various clinical and pharmaceutica companies.* Experienced in generating and validation of Tables, Listings, Graphs and performing ADHOC analysis.* Expertise in generating safety and efficacy study reports for CSR, ISS and ISE for NDA submissions* Proficient in using various SAS programming modules including SAS/BASE,SAS/STAT,SAS/GRAPH, SAS/MACRO and SAS/SQL in both UNIX and Windows environments.* Extensive work experience in creating SDTM, ADAM datasets following CDISC standards for regulatory submissions and also doing the Gap analysis.* Strong knowledge in documenting and reporting validation inspections in compliance with 21 CFR part II guidelines.* Extensive exposure to SAS programming, merging SAS Data Sets, Macro Facility, preparing and manipulating Data sets, Statistical procedures, producing reports etc.* Excellent knowledge of statistical procedures like PROC REPORT, PROC FREQ, PROC MEANS, PROC UNIVARIATE, PROC MIXED, PROC GLM, PROC LIFETEST, PROC PHREG.* Experience in working for data management support programming and generating data cleaning reports.* Gained experience in analyzing clinic trials data in therapeutic areas including Gastrointestinal, Neuroscience, Cardiovascular, Allergy, Immunology, Bunionectomyand other diseases.* Strong command on clinical drug development process and all the phases of clinical trial from preclinical to post market studies.