I'm a member of the Hollings Cancer Center Biostatistics Shares Resource. The majority of my time is spent collaborating with cancer researchers on study designs, sample size considerations, statistical analysis/plans, and grant and manuscript preparation. Projects range from small scale pilot and basic science studies to larger randomized clinical trials. Additionally, I worked several years in the pharmaceutical industry and have a great deal of experience with drug stability studies, laboratory QC best practices, and assay validation and optimization. I have authored and/or co-authored statistical sections of regulatory filings and several peer-reviewed journal articles.