Tanya
Green
Senior Vice President, Chief of Staff
Tanya Green
Senior Vice President, Chief of Staff
Tanya Green brings more than 20 years of biopharmaceutical industry leadership experience, with a strong track record of clinical development and commercialization. Throughout her career, she has successfully secured numerous regulatory approvals for rare disease and oncology therapies, including AYVAKIT®, GAVRETO®, CERDELGA® and KANUMA®. Since joining Blueprint Medicines in January 2017 as Director of Regulatory Affairs, Tanya has played a pivotal role in the company’s success. She served as the regulatory lead on the avapritinib program, obtaining the company’s first regulatory approval. In March 2020, Tanya was appointed Head of Global Regulatory Sciences and subsequently Senior Vice President, where she was integral in building a diverse, high-growth global organization while fostering a strong company culture. Previously, Tanya held regulatory affairs roles at Alexion and Genzyme. She holds a B.S. in Biology from Suffolk University and an M.S. in Regulatory Affairs and Health Policy from the Massachusetts College of Pharmacy and Health Sciences.