25+ years of clinical research experience; member of Society for Clinical Data Management and eClinical Forum; CDISC. TA experience: Oncology (including I-O), Cardiovascular, Immunology, Virology, and Neuroscience.

Multi-talented pharmaceutical professional with recognized, comprehensive expertise in data management, clinical trial execution, and initiative implementation, capitalizing on diverse experience in large pharma, biotech, small business, and CRO organizations; proficiency across clinical development including study management, data management, and inspection response; active participant in numerous audits, inspections, and quality investigations which included the development, execution, and tracking of Corrective Action and Preventative Action (CAPA) plans; demonstrated aptitude for quickly mastering new technologies; superior performance in deadline-driven environments; confidence in interactions with professionals and non-professionals at all levels; ability to translate business requirements into technology solutions and to translate technological capabilities and limitations into business possibilities.