Prior to joining GreenLight Clinical, Michael has worked over 20 years within the pharmaceutical industry in a variety of R&D positions, primarily within Clinical Operations. His experience includes both large and small pharmaceutical and biotech sponsors where he was responsible for all aspects of protocol feasibility, development, including program country strategy, protocol optimization, enrollment modeling, investigator strategy and assessment of competitive landscape. Having experience within organizations such as Achillion Pharmaceuticals, Pharmasset/Gilead, Altana Pharma and Schering-Plough, has given Michael unique insight into systemic blind spots sponsors have regarding clinical research and operations. Michael’s extensive years of experience have afforded him the opportunity to work with many laboratories, clinical packaging, data management, investigators, study teams, and CROs with the initiative to apply these skills strategically and innovatively to address complex issues. Michael earned his Bachelor of Science degree in Biology from Rowan University and a Master of Science in Regulatory Affairs and Quality Assurance from the Temple University School of Pharmacy.