Celeste Carey

Celeste Carey is a skilled professional in clinical research and drug product development with extensive experience at Dana-Farber Cancer Institute and Biogen. Currently serving as CTO Research Project Manager I for Lymphoma Clinical Trials, Celeste oversees project management, Trial Master File maintenance, protocol development, and research project phases. Previous roles at Dana-Farber included Clinical Regulatory Coordinator II and I, focusing on regulatory approvals, file maintenance, and stakeholder collaboration. At Biogen, Celeste held positions as Associate Scientist III and II, executing formulation studies and authoring reports. Celeste's educational background includes a Professional Master of Science in Biotechnology from Northeastern University and a Bachelor of Science in Biological Sciences from the University of Rhode Island.