Jessica Smith Beaver

Jessica Smith Beaver

Head Of Regulatory Affairs @ Mindstate Design Labs

About Jessica Smith Beaver

Jessica Smith Beaver is the Head of Regulatory Affairs, with a strong background in pharmacokinetics and drug metabolism, and extensive experience in regulatory roles across various pharmaceutical companies.

Jessica Smith Beaver: Head of Regulatory Affairs

Jessica Smith Beaver is currently the Head of Regulatory Affairs. She has accumulated a wealth of experience in the field through various senior roles in notable companies. Her expertise lies in ensuring compliance and navigating the complex landscape of regulatory requirements in the pharmaceuticals industry.

Jessica Smith Beaver's Education and Expertise in Pharmacokinetics and Law

Jessica Smith Beaver holds a PhD in Pharmacokinetics & Drug Metabolism from the University of North Carolina at Chapel Hill, providing her with deep scientific knowledge crucial for the pharmaceuticals sector. Additionally, she earned a Master of Legal Studies in Business & Compliance Law from Washington University in St. Louis. This combination of scientific and legal expertise equips her to adeptly manage regulatory complexities within the industry.

Jessica Smith Beaver's Career at Johnson & Johnson

Jessica Smith Beaver began her career at Johnson & Johnson, where she served as a Clinical Pharmacokinetics Leader. In this role, she applied her in-depth knowledge of pharmacokinetics to lead projects related to drug metabolism, ensuring that clinical practices met the highest standards of efficacy and safety.

Jessica Smith Beaver's Roles at Targacept, Kowa Pharmaceuticals, and Verinetics

Jessica Smith Beaver has held senior regulatory roles at Targacept, Kowa Pharmaceuticals, and Verinetics. Her responsibilities at these companies included overseeing regulatory compliance, developing strategies for regulatory submissions, and ensuring products met all necessary legal and safety standards. Her diverse experience across these firms has solidified her status as an expert in regulatory affairs within the pharmaceuticals industry.

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