Adam Barrows
About Adam Barrows
Adam Barrows is the Sr. Director and Solid Tumor TA Head of Development at Bristol Myers Squibb, with extensive experience in clinical trials and therapeutic areas including oncology and cardiovascular diseases.
Current Position at Bristol Myers Squibb
Adam Barrows is currently serving as the Senior Director of Solid Tumor TA Head in Development at Bristol Myers Squibb. He began this role on April 1, 2020. His responsibilities include overseeing the strategy and management of development activities focused on solid tumor therapies. His expertise in this area is leveraged to bring life-saving medicines to patients in need, enhancing the company's oncology pipeline.
Previous Roles at Bristol Myers Squibb
Before his current role, Adam Barrows held various positions at Bristol Myers Squibb. From 2019 to 2020, he was the Clinical Trial Lead/Study Director in Princeton, New Jersey. Prior to that, he was the Associate Director, Protocol Management Line Manager from 2017 to 2019 and the Protocol Manager from 2016 to 2017. These roles have provided him with extensive experience in clinical trial design, management, and execution.
Experience at MedAvante, Inc.
Adam Barrows worked as a Senior Project Manager at MedAvante, Inc. from 2011 to 2016. During his five-year tenure, he managed various clinical projects, gaining valuable experience in project management within the clinical research field. His role involved coordinating multiple aspects of clinical studies, contributing to the successful execution of these projects.
Educational Background
Adam Barrows has a strong educational foundation. He earned his Bachelor of Science in Biology/Pre-Med/French from Albright College. Additionally, he holds a Master of Business Administration (MBA) from the University of Delaware. This education has equipped him with a comprehensive understanding of both scientific and business aspects, crucial for his roles in clinical development and project management.
Early Career Experience
Adam Barrows started his career with various roles that provided him with a broad range of experiences. He worked as a Clinical Studies Associate/Clinical Data Coordinator at ICON Clinical Research and as a Clinical Trial Associate at inVentiv Health/Wyeth. He also held positions such as College Admission Counselor at Albright College and Clinical Nursing Assistant at Reading Hospital and Medical Center. These roles helped him build a strong foundation in clinical research and project management.