Merck
Elizabeth Duffey Rodier, MS, is an Associate Director and Regulatory Submissions Manager at Merck since December 2020, previously serving as a Senior Specialist in the same department. Prior experience includes work at Fox Chase Cancer Center from July 2017 to December 2020 as a Regulatory Trial Lead and Regulatory Coordinator, where responsibilities encompassed the compilation and submission of protocols to regulatory bodies and maintaining compliance with regulatory standards. Elizabeth holds a Master’s Degree in Regulatory Affairs and Quality Assurance from Temple University School of Pharmacy and a Bachelor of Science in Behavioral Aspects of Health from the University of Delaware.
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