Experience in SAS (9.1.3) windows and UNIX environment Good working knowledge in different domains of clinical trials data like demographic data, adverse event, protocol deviations and violations, laboratory data, physical exam, medical History and vital signs etc., Good experience in developing and validating SAS Macros Strong knowledge in all phases of clinical trials and 21CFR Part II regulations Experience in leading and managing a team Team Player with strong numerical, Problem solving and analytical skills Work experience in developing & validating SDTM, ADaM datasets and patient profiles Excellent Interpersonal skills and decision making skills with a positive approach Self motivated, hardworking, dedicated with ability to understand and meet the time lines Actively Involved in recruitments like taking technical interviews Good comprehension of FDA and CDISC guidelines, Good Clinical Practice (GCP) Developed general utility macros using SAS & VBA to automate the process Onsite work experience in OCKHAM Clinical Research in Cary, North Carolina Certificate of appreciation towards production and quality on Sep 2012 in ACCENTURE