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Hurley is responsible for regulatory affairs clinical compliance and drug safety surveillance. Dr. Hurley has over 20 years of regulatory and project management experience in the biotechnology and pharmaceutical industry. Most recently Dr. Hurley served as Vice President Regulatory Affairs for Neose Technologies Inc. At Neose Dr. Hurley managed the strategy and execution of interactions with the FDA as well as the quality assurance and project management functions. Prior to Neose Dr. Hurley served as Assistant Director Regulatory Sciences at Cytogen Corporation. While at Cytogen Dr. Hurley was responsible for regulatory submissions clinical compliance and project management functions. She served as the Company spokesperson with the FDA and European partner on all aspects of the regulatory process. Marjorie received her Pharm.D. and B.S. in Pharmacy from the University of Michigan. | 