Bridging rigorous scientific training, international leadership, and hands-on operational execution to guide your drug development programs from concept to clinic.
I benefited from the French educational model which emphasizes a broad, multidisciplinary foundation spanning both scientific and non-scientific domains up to age 18, followed by broad scientific university training encompassing mathematics, computing, physics, chemistry, and biology well into Master's level studies. This broad curriculum provides a uniquely versatile framework, enabling me to fluidly interact with specialists across diverse domains and effectively bridge the gap between preclinical scientists, clinical operations teams, and commercial stakeholders.
This multidisciplinary foundation is complemented by advanced academic training from a top-tier European university, with a PhD in Organic Chemistry from the University of Oxford. This combination ensures a uniquely broad yet deeply analytical approach when evaluating complex data packages, trial designs, and regulatory dossiers.
Building upon these roots, my career spans professional leadership roles across the UK, the US, Australia, Switzerland, and France alongside daily collaboration with cross-functional teams in India, China, and broader Asia. This multicultural exposure allows me to navigate diverse environments and align stakeholders seamlessly, regardless of geography or organizational culture.
My career reflects a rare breadth of exposure across large pharmaceutical companies, biotech, not-for-profit organizations, contract research organizations (CROs), and international product development partnerships—giving me a deep, first-hand understanding of the unique bottlenecks, regulatory nuances, and operational pressures clients face at every stage.