Marc Ippolito
About Marc Ippolito
Marc Ippolito is the Regional Clinical Compliance Lead - Americas at Bristol-Myers Squibb in Princeton, New Jersey, with extensive experience in clinical trial management and compliance oversight.
Current Role at Bristol-Myers Squibb
Marc Ippolito currently serves as the Regional Clinical Compliance Lead for the Americas at Bristol-Myers Squibb. Based in Princeton, New Jersey, he is responsible for overseeing clinical compliance initiatives across the region. He ensures that all clinical trials adhere to regulatory standards and organizational protocols.
Previous Roles at Bristol-Myers Squibb
Before his current role, Marc Ippolito worked as a Senior Clinical Protocol Manager at Bristol-Myers Squibb. During his tenure from 2015 to 2018, he managed clinical protocol design and CRF design for various trials. His responsibilities also included developing recruitment plans and providing mentorship to team members.
Experience at Pfizer
Marc Ippolito spent four years at Pfizer, where he held the position of Associate Director - Compliance Oversight Lead from 2011 to 2015. In this role, he focused on quality monitoring oversight and audit/inspection readiness, ensuring compliance with regulatory requirements. He also previously served as an FSP Study Manager from 2007 to 2008 in New York, NY, overseeing various study management tasks.
Educational Background
Marc Ippolito holds a Bachelor of Science degree in Psychology and Neuroscience from the University of Massachusetts Amherst, which he earned between 1992 and 1995. His educational foundation has been instrumental in shaping his expertise in clinical research and trial management.
Industry Expertise and Skills
Marc Ippolito has extensive expertise in managing clinical trial budgets and global supply logistics. He specializes in protocol design, CRF design, and recruitment planning. He is also experienced in quality monitoring oversight, large multi-national mega-trials, and continuous improvement initiatives. Additional competencies include global site management, vendor management, compliance, and audit/inspection readiness.