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Karen Y. serves as the Associate Director of Regulatory Affairs and Medical Writing at BlueRock Therapeutics, focusing on global regulatory strategies and medical writing for advanced cell therapies targeting Parkinson's disease. Previously, Karen held the role of Senior Manager in both Regulatory Affairs and Medical Writing at BlueRock, where responsibilities included developing clinical deliverables and enhancing operational efficiency through standardization. At Lundbeck, Karen was Senior Manager of Medical Affairs, where contributions involved strategic planning, team leadership, and lifecycle management across multiple psychiatric products. Additionally, as an Innovation Consultant at The Savvy Scientist, LLC, Karen led global collaborations for Fortune 500 companies, creating solutions that garnered recognition. Karen holds a PhD and MS in Molecular Toxicology from UCLA and a BS in Biology from the University of Illinois Urbana-Champaign.