Adam Bone is a seasoned professional with 25 years of experience in regulatory affairs. They have held various roles, including Regulatory Aff airs Manager II at Biogen since 2025, and previously served as a Regulatory Submission Manager and Clinical Publishing Specialist at Merck from 2021 to 2023. Adam began their career as a Technical Writer at Ortho Clinical Diagnostics from 1996 to 2004, and later worked at Bristol-Myers Squibb and Sanofi-Aventis. Adam holds a Bachelor of Arts in Criminal Justice and Corrections from Richard Stockton College of New Jersey and an Associate degree in Communications from Mercer County Community College.
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