Gerrit S. Hamre MA

Research Project Manager, Clinical Trials Transformation Initiative, Duke University

Mr. Hamre manages the development and implementation of CTTI projects. In collaboration with team leaders, he creates project plans and budgets, and manages the implementation of project plans.

Mr. Hamre has more than ten years of experience in the pharmaceutical industry, including regulatory, legislative, and business management work. Four years prior to joining CTTI, he worked in the Food and Drug Administrations (FDA) Office of Legislation, followed by the FDAs Center for Drug Evaluation and Research, Office of Policy for Pharmaceutical Quality. His primary areas of focus at the FDA were the drug approval process, antibacterial drug development, manufacturing quality, and generic drugs. Before joining the FDA, Mr. Hamre worked on pharmaceutical science or healthcare delivery administration issues in corporate, federal government, and non-government organization (NGO) sectors, domestically and internationally. Mr. Hamre is also a returned Peace Corps Volunteer; he served in South Africa from 2004 to 2006.


This speaker has made no appearances.