Leila Mamirova

Leila Mamirova, PhD, is an Associate Regulatory Program Director at Roche, where they leverage over a decade of experience in Regulatory Affairs and CMC Project Management, with a foundation in clinical research. They previously held roles as a Senior Project Manager and Technical Regulatory Manager at Roche and have rich experience as a Project Manager in biotechnology and regulatory departments at Stragen and Celonic Group. Leila earned their PhD in Bioinformatics and an MSc in Biochemistry from Lomonosov Moscow State University.