Michael Phillips
About Michael Phillips
Michael Phillips is a Regulatory Affairs Associate II at Supernus Pharmaceuticals, Inc., where he has worked since 2021. He has a background in research coordination and regulatory compliance, with previous roles at Johns Hopkins School of Medicine and the American Academy of Otolaryngology.
Work at Supernus Pharmaceuticals
Michael Phillips has been employed at Supernus Pharmaceuticals, Inc. as a Regulatory Affairs Associate II since 2021. In this role, he is responsible for reviewing and submitting advertising promotional materials to ensure compliance with regulatory standards. He also compiles Investigational New Drug (IND) annual reports and prepares labeling supplements as part of his regulatory duties. His work contributes to maintaining regulatory compliance within the pharmaceutical industry.
Previous Experience in Regulatory Affairs
Prior to joining Supernus Pharmaceuticals, Michael Phillips worked as an Analyst in Quality & Performance Measurement at the American Academy of Otolaryngology from 2020 to 2021. He also served as a Research Program Coordinator at Johns Hopkins School of Medicine from 2016 to 2020. In these roles, he gained experience in regulatory compliance and project coordination, which are essential for his current position.
Education and Expertise
Michael Phillips holds a Master of Health Science degree in Mental Health from the Johns Hopkins Bloomberg School of Public Health, which he completed in 2020. He also earned a Bachelor's Degree in Psychology from the University of Maryland Baltimore County in 2015. Additionally, he has an Associate's Degree in General Studies from Howard Community College, obtained in 2012. His educational background supports his expertise in regulatory affairs and health sciences.
Background in Research and Coordination
Michael Phillips has a background in research and program coordination. He worked as a Research Assistant at the University of Maryland Baltimore County from 2014 to 2015 and as a Research Program Coordinator at Johns Hopkins School of Medicine from 2016 to 2020. These positions involved coordinating research projects and managing data, which provided him with valuable skills applicable to his regulatory affairs role.
Contributions to Regulatory Compliance
In his current role and previous positions, Michael Phillips has contributed to regulatory compliance by creating sample loss reports and submitting them to the FDA. He also coordinates product labeling, playing a significant role in the regulatory aspects of drug discovery projects. His efforts ensure that the products meet the necessary regulatory standards.