I hold a Ph.D. in Biostatistics from UNC - Chapel Hill. I worked at GSK for the past 15 years before moving to Parexel. I have held a number of different positions. I started out in the non-clinical statistics group supporting inhalation product development, working with engineers who make devices for respiratory diseases. After two years, I moved to a clinical statistics group, supporting clinical pharmacology trials. I worked on trials in HIV and Hepatitis C as well as a few in metabolic disease areas. Later, I moved to Oncology where I worked for most of the past 7 years, supporting first-time-in-human and Phase II trials in Oncology. I have been the lead statistician for a number of different compounds including one that was submitted to the FDA. Recently I moved to supporting Respiratory late-phase clinical trials. I have designed several Bayesian clinical trials and am active with the ASA. I previously surpervised a number of student interns from NC State University. I have also taught several training courses in statistics while at GSK.

Associate Director, Biostatistics @ Provide statistical support for clinical trials in the Respiratory therapy area. From March 2015 to Present (10 months) Manager, Statistics @ Provide statistical consulting and support to clinical colleagues. Represent Clinical Statistics on project teams. Responsible for study design, statistical sections and general review of study protocols, authorship of Reporting and Analysis Plans (RAPs), oversight of programming of statistical displays for study reports, and statistical aspects and general review of study reports. Oversee outsourced work as needed. Supervised graduate student interns from NC State and UNC from 2006-2011. From November 1999 to March 2015 (15 years 5 months) Statistician III / Research Assistant Professor @ Analyzed and managed data for the North Carolina Colon Cancer Study and other studies conducted by the Center for Gastro-Intestinal Biology and Disease (CGIBD). Prepared statistical sections of grant proposals and journal articles. Supervised data entry and data management staff. Consulted with fellows and members of the CGIBD. From 1993 to 1999 (6 years)

MS., Ph.D., Biostatistics @ UNC Chapel Hill From 1984 to 1990 B.A., Statistics @ University of Michigan From 1982 to 1984 Sharon Murray is skilled in: Clinical Trials, Oncology, Biostatistics, Clinical Study Design, Clinical Development, Clinical Research, Pharmaceutical Industry, Protocol, CRO, Statistics, Drug Development, SAS, Survival Analysis, FDA, GCP, Regulatory Submissions, Biotechnology, Infectious Diseases, Clinical Pharmacology