Over 2 years of programming experience in developing and implementing various applications for the pharmaceutical, clinical and health industries. Experience includes creation of analysis datasets, good experience with CDISC models such as SDTM, and involved in Clinical Trails Phase(I-IV)
Summary:

? Extensive work experience in Clinical Data Management, Data Analysis, and generating Reports, Tables, Listings, CRT’s (Case Report Tabulation), and Summaries from clinical trial data and In-depth knowledge of statistical analysis techniques and excellent experience in analyzing safety data for clinical trials.
? SAS programming experience in generating Analysis Datasets/SDTM
? Good understanding of CRT (Item 11) dataset creation, CDISC, MedDRA, ICH Guidelines, GCP, NDA, 21CFR PART 11 Rules and Regulations for regulatory submissions.
? Strong working knowledge of different phases of clinical trials data like Demographic data, Adverse event, Disposition, Exposure, Concomitant Medication, Medical History, laboratory data, vital signs etc .
? Proficiency in various SAS tools like SAS/Base, SAS/STAT and excellent working knowledge of SAS Procs like proc report, proc freq, proc means, proc tabulate, proc chart, proc contents, proc dataset, proc format, proc import, proc export, proc print, and Proc UNIVARIATE.
? Extensively used SAS/MACRO for creating macro variables and macro programs to modify existing SAS program for ease of modification while maintaining consistency of results and also developed SAS/ Macros for generic coding and reusable modules.
? Good experience in storing and manipulating data in SAS files by Merging, Formats, Informats, SQL Joins and Proc Transpose.
? Experienced in producing Excel, RTF, HTML and PDF formatted files using SAS ODS.
? Excellent communication and interpersonal skills and accustomed to working in challenging environments and a good team player.
? Extensive experience as a SAS Programmer in Windows & UNIX platforms and expert to aut