ÂÜÀòÂÒÂ×

Rosy Lambert is an accomplished regulatory affairs professional with extensive experience in the biotechnology and pharmaceutical industries. Currently serving as Senior Manager of Regulatory Affairs at AVEO Oncology since May 2022, Rosy has a robust background that includes positions such as Manager of Regulatory Affairs at Inozyme Pharma and Senior Regulatory Affairs Specialist at Akebia Therapeutics. Prior roles also include Senior Clinical Trial Associate at Takeda, Clinical Trial Associate at ARIAD Pharmaceuticals, Trial Master File Associate at Vertex Pharmaceuticals, and Study File Analyst at Biogen. Rosy's educational background includes a Bachelor's degree in Biomedical Laboratory and Clinical Sciences from Boston University and a Master's degree in Regulatory Affairs from Northeastern University.