Youness A. is currently the Regulatory Associate Program Director at Roche, where they focus on strategic and submission-related activities for oncology product development. They previously held positions as a European Project Manager at ANSM and as a Scientific and Regulatory Trainee at the European Medicines Agency. Youness earned a Doctor of Pharmacy and a Master 2 in European and International Regulatory Affairs of Health Products, establishing a strong foundation for their career in regulatory affairs. Their extensive experience includes managing clinical trials, assisting in marketing authorization processes, and coordinating cross-functional policy meetings.
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