Mark Reynard
About Mark Reynard
Mark Reynard is a Regulatory Affairs Manager at Bristol Myers Squibb in New Jersey, with over two decades of experience in the pharmaceutical and healthcare sectors, specializing in regulatory affairs and compliance.
Current Role at Bristol-Myers Squibb
Mark Reynard is currently employed as a Regulatory Affairs Manager at Bristol-Myers Squibb in New Jersey, United States. Bristol-Myers Squibb is a global biopharmaceutical company that focuses on scientific excellence and innovation in biopharmaceutical research. The company offers a range of products in areas such as oncology, cardiovascular, and immunology, and actively supports patient access to medications through various programs and initiatives.
Previous Experience at GSK
Mark Reynard has a significant professional history with GSK, having worked in multiple roles. He served as the Asia Regulatory Compliance Manager for six months in 2015. Prior to that, he worked as a Therapy Project Manager and Regulatory Affairs Manager for five years from 2011 to 2016. Mark also held the role of Senior Regulatory Associate for five months in 2011. His initial roles at GSK included Lead Clinical Scientist from 2001 to 2007 and Submissions Consultant from 2001 to 2005 in Hayes, Hillingdon, United Kingdom.
Experience in Clinical Science at Roche
Before his tenure at GSK, Mark Reynard worked as a Clinical Scientist at Roche in Switzerland from 2007 to 2011. In this role, he was involved in various clinical research and development activities, leveraging his strong background in clinical science. His work at Roche contributed to his extensive expertise in the pharmaceutical industry, particularly in regulatory affairs and compliance.
Educational Background
Mark Reynard holds a Doctor of Philosophy (Ph.D.) from the University of London, which he earned from 1998 to 2001. Additionally, he completed a Bachelor of Science (B.Sc.) degree at the University of Leeds from 1995 to 1998. His academic background laid the foundation for his extensive career in clinical science and regulatory affairs within the pharmaceutical sector.
Extensive Experience in Regulatory Affairs and Compliance
Mark Reynard has more than two decades of experience in the pharmaceutical and healthcare sectors, with a particular focus on regulatory affairs and compliance. He has worked on regulatory submissions and compliance for multiple regions, including Asia and Europe. His career showcases a diverse skill set, transitioning from clinical science roles to regulatory affairs, which highlights his comprehensive understanding of the pharmaceutical industry's regulatory landscape.