James Courmarcel
About James Courmarcel
James Courmarcel is the Associate Director of European Regulatory Procedure Management at Bristol Myers Squibb, with over 15 years of experience in regulatory coordination and global documentation.
Current Role at Bristol Myers Squibb
James Courmarcel serves as the Associate Director, European Regulatory Procedure Management at Bristol Myers Squibb (BMS) in Braine-L'alleud. In this capacity, he oversees regulatory procedures across European markets, ensuring compliance with regional requirements and contributing to the successful management of regulatory documentation and processes. This role capitalizes on his extensive experience within BMS and his deep understanding of both the regulatory landscape and global documentation.
Previous Roles at Bristol Myers Squibb
James Courmarcel has held several positions at Bristol Myers Squibb over his 15-year tenure. He began as a Dossier Specialist in Global Documentation and Dossier Management (2005-2007), before being promoted to Sr Dossier Specialist (2007-2008). He then served as Sr European Regulatory Coordinator (2008-2010) and Manager of European Regulatory Coordination (2011-2014). These roles provided him with a solid foundation in documentation, dossier management, and regulatory coordination, leading to his current senior position.
Educational Background in Chemistry
James Courmarcel holds a PhD in Organometallic Chemistry and Catalysis from Université catholique de Louvain, completed from 2000 to 2003. Following his PhD, he pursued a Post-Doctoral fellowship at Universitat Autònoma de Barcelona in a similar field, focusing on Organometallic Chemistry and Catalysis between 2004 and 2005. His academic credentials underscore a strong background in chemistry, which complements his regulatory expertise in the pharmaceutical industry.
Experience in Global Documentation and Dossier Management
With over 15 years at Bristol Myers Squibb, James Courmarcel has accumulated extensive experience in global documentation and dossier management. Starting as a Dossier Specialist and progressing to senior roles, he has been integral in managing the complex regulatory and documentation processes critical to the pharmaceutical industry. This experience is essential for his current role, where he oversees European regulatory procedures.
Contributions to European Regulatory Landscape
Based in the Brussels Metropolitan Area, James Courmarcel plays a significant role in shaping and managing Bristol Myers Squibb's European regulatory landscape. His work involves navigating the intricate regulations across different European markets, ensuring compliance, and facilitating the approval of important pharmaceutical products. His contributions are vital in maintaining BMS's regulatory standards and market presence in Europe.