Brooke Dapolito, MBA has worked in various roles throughout their career. Brooke is currently the Director of Regulatory Project Management at Athersys, a position they have held since August 2021. Prior to this, they served as the Associate Director of Project Direction at Delcath Systems, Inc from April 2021 to August 2021. From January 2020 to April 2021, Brooke worked as a Senior Manager of Submissions and Project Management at PRA Health Sciences.
Before joining PRA Health Sciences, Brooke had an extensive tenure at Pfizer. Brooke worked as a Senior Project Manager in the Project Portfolio Management division from April 2019 to January 2020. Previously, they held the position of Manager of Global Regulatory Submissions from March 2017 to April 2019. Brooke's responsibilities in these roles focused on overseeing the development and submission of regulatory documents.
Brooke's career at Pfizer began in July 2013 when they joined as an Associate Scientist in the Conjugates and Polytides Process Development group. In this role, they were involved in the manufacturing process development for bioconjugate pharmaceuticals. Subsequently, they became a Senior Associate in ADC Operations, where they operated the drug product Fill Finish line for Antibody Drug Conjugates.
Before their time at Pfizer, Brooke gained experience as a Research Intern at MilliporeSigma from June 2012 to May 2013. Brooke also had a Summer Internship at Travelers in 2010, where they worked on the testing and implementation of a Document Repository system.
Brooke Dapolito's diverse work experience showcases their expertise in project management, regulatory submissions, and pharmaceutical manufacturing processes.
Brooke Dapolito, MBA, received a Bachelor of Science (BS) degree in Biochemistry from Worcester Polytechnic Institute in 2013. Brooke then pursued further education and completed their Master of Business Administration (M.B.A.) in Business Administration and Management, General from Iona University between 2015 and 2017.
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