Cécile Bertin

Cécile holds a Pharm.D and a Master’s in International Drug Development and Registration. She joined Roche headquarters in Basel in 2015, first as a trainee and then as a post graduate. She currently works as an Associate Regulatory Program Manager in the Oncology Department. Her daily mission is to work with the development teams to design, implement innovative regulatory strategies, driving the cross-functional teams to accelerate development of medicinal products. Cécile has been supporting the Leader of Tomorrow activities for DIA Europe 2018 and 2019.