Dan Soroko

Dan Soroko currently serves as Senior Director of Regulatory Affairs at Sage Therapeutics, a position held since February 2017. Previously, Dan held various roles at Biogen, including Director of Regulatory Affairs, where responsibilities included directing global regulatory strategies for clinical development. Experience also includes the role of Senior Manager of Regulatory Affairs at Acceleron Pharma, focusing on regulatory strategies in oncology and hematology, and significant contributions at Genzyme and Wyeth in supporting global clinical programs. Early in the career, Dan managed clinical trials at Joslin Diabetes Center. Academic qualifications include a BA from Brandeis University and an MS from the Massachusetts College of Pharmacy and Health Sciences.