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Anna Marie Beckmann, PhD
Vice President, Product Development & Regulatory Affairs
Anna Marie Beckmann is the Vice President of Product
Development and Regulatory Affairs at IDRI. She is
responsible for guiding products through the transitional
phase from pre-clinical research to evaluation in clinical
trials. In the regulatory affairs arena, her group provides the
necessary documentation to the U.S. Food and Drug
Administration for review and approval of IDRI's vaccine and
adjuvant candidates in human clinical trials. She is also
responsible for IDRI's in-house pilot manufacturing facility
that produces cGMP adjuvant formulations for Phase 1
vaccine clinical trials.
Anna Marie was a Senior Fellow in the STD Training
Program at the University of Washington and a faculty
member at the Fred Hutchinson Cancer Research Center,
where her research focused on the pathogenesis of human
papillomavirus infections (HPV) and the relationship between
HPV infections and human anogenital cancers. In 1998 she
joined Corixa Corporation as Director of Regulatory Affairs
and worked on early stage clinical development of vaccines
for infectious diseases and cancer.
Anna Marie Beckmann earned her PhD from the Department
of Immunology and Infectious Diseases at Johns Hopkins
University School of Public Health. Her thesis was focused
on the pathobiology of infection with the human
papillomaviruses JC and BK.
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