Brooke Dapolito

She is a regulatory project management and pharmaceutical development professional with experience in regulatory submissions, project direction, bioconjugate process development, and antibody drug conjugate operations. She currently serves as Director of Regulatory Project Management at Athersys in Cleveland, Ohio. Her background includes project management roles with Delcath Systems, PRA Health Sciences, and Pfizer, where she supported global regulatory submissions, manufacturing operations, and process development. She also gained research experience at MilliporeSigma, focusing on monoclonal antibody purification.