VP, Head, Global Regulatory Affairs @ GlaxoSmithKline Vaccines
Vice President, Global Reg Strategy, Immunotherapeutics @ GlaxoSmithKline (GSK)
Executive Director (Sr. Director/Director), US Regulatory Affairs Pediatric Vaccines @ GlaxoSmmithKline
Education:
B.S. @
Penn State University
About:
VP, Head, Global Regulatory Affairs @ Oversee/Direct strategy, operations and global regulatory team for entire GSK Vaccines portfolio From January 2015 to Present (1 year) Greater Philadelphia AreaVice President, Global Reg Strategy, Immunotherapeutics @ Oversee regulatory strategy and operations for development and commercialization of therapeutic vaccines for cancer and chronic disorders global markets. From January 1996 to
VP, Head, Global Regulatory Affairs @ Oversee/Direct strategy, operations and global regulatory team for entire GSK Vaccines portfolio From January 2015 to Present (1 year) Greater Philadelphia AreaVice President, Global Reg Strategy, Immunotherapeutics @ Oversee regulatory strategy and operations for development and commercialization of therapeutic vaccines for cancer and chronic disorders global markets. From January 1996 to December 2014 (19 years) Executive Director (Sr. Director/Director), US Regulatory Affairs Pediatric Vaccines @ From February 1998 to December 2006 (8 years 11 months) Microbiologist, Chief, Branch I, DEL & Associate Director, OELPS @ Applied laboratory research; reviewer of investigational product applications; reviewer of market applications; inspector of production facilities; policy maker; manager - for variety of biological/biotechnology products From August 1987 to January 1996 (8 years 6 months)
M.S., Biotechnology @ The Johns Hopkins University From 1993 to 1995 B.S., Microbiology @ Penn State University From 1983 to 1987 B.S., Microbiology @ The Pennsylvania State University - Main Campus From 1983 to 1987 Haddonfield Memorial High School From 1979 to 1983 Amy Scott is skilled in: Regulatory Affairs, Biotechnology, Vaccines, Pharmaceutical Industry, FDA, Biopharmaceuticals, Clinical Development, Regulatory Submissions, GMP, Lifesciences, IND, Technology Transfer, Clinical Trials, Drug Development, Validation, Oncology, Regulatory Requirements, Biologics
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