What I do at MMV:

My role is to provide regulatory support and manage regulatory activities for selected projects and activities across the MMV portfolio in collaboration with the project teams and partners.

Why I work at MMV:

It is exciting and a privilege to be part of an organisation that develops the next generation of drugs to address the unmet medical needs of vulnerable people at risk of malaria and to hopefully lead to eradication of this devastating disease. Having worked in the pharmaceutical industry for the past 15 years, I would like to use my experience and skills to contribute to this effort at MMV.

More about me:

I hold a Doctor of Pharmacy and a post-graduate diploma in Regulatory Affairs from the University of Lyon. Prior to joining MMV in 2022, I worked at GeNeuro SA, Novartis Consumer Health and Merck Serono where I gained experience on global development and international registrations of both chemical and biotechnology products.

Ask me about:

Regulatory submissions including Clinical Trial Applications and Marketing Authorisation Applications, eCTD.