Peter Marks | |
---|---|
Director of the Center for Biologics Evaluation and Research | |
Assumed office 2016 | |
President | Barack Obama Donald Trump Joe Biden |
Preceded by | Karen Midthun |
Personal details | |
Education | Columbia University (BS) New York University (MD,PhD) |
Scientific career | |
Fields | Oncology |
Institutions | Brigham and Women's Hospital Yale University |
Doctoral advisor | Frederick R. Maxfield |
Peter Marks is an American hematologist oncologist serving as the director of the Center for Biologics Evaluation and Research within the Food and Drug Administration. He was appointed to the position in 2016 after previously serving as deputy director.
Marks earned a Bachelor of Science degree from Columbia University,followed by a Doctor of Medicine and PhD in cell and molecular biology from New York University in the lab of Fredrick R. Maxfield. As an undergraduate,he volunteered at Mount Sinai St. Luke's in New York City,where he worked in the radioimmunoassay lab. He completed an internal medicine residency and oncology training at the Brigham and Women's Hospital. [1] [2]
After completing his training,Marks worked at the Brigham and Women's Hospital as a clinician-scientist,and later served as Clinical Director of Hematology. He then worked in the pharmaceutical industry,where he worked on the development of hematology and oncology products. He later managed the Adult Leukemia Service at Yale University and served as the Chief Clinical Officer of the Yale New Haven Hospital Cancer Center. Marks joined the Center for Biologics Evaluation and Research as deputy director in 2012,and was promoted to director in 2016. [3] [4]
In May 2020,he was selected to serve as a member of the White House Coronavirus Task Force, [5] although he left a few days later over concerns that his participation would represent a conflict with his position at FDA. [6] Marks also played a role in establishing Operation Warp Speed,a partnership between the federal government and various private companies to develop a COVID-19 vaccine,but left the project in May 2020 shortly after it was launched. Marks believed he would be more useful in his role as chief regulator of vaccines as the Director of FDA's Center for Biologics Evaluation and Research. [7] [8] [9] In 2021,Marks served as a plenary speaker at the State of the Science Research Summit. [10] In 2024,Marks overruled FDA staff to approve gene pharmacotherapy Elevidys—intended to treat Duchenne muscular dystrophy—despite it failing in Phase III clinical trial. [11]
Marks has two children and resides in Washington,D.C.,with his wife. [12]
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