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Drug Safety and Pharmacovigilance Across the Product Lifecycle

Build a solid foundation in the key concepts of drug safety and pharmacovigilance throughout the medical product development lifecycle. Learn how to comply with regulatory requirements.


Faculty

  • Jill W. Buckley, PharmD

    Jill W. Buckley, PharmD

    • Adjunct Assistant Professor
    • Rutgers, the State University of New Jersey, United States

    Dr. Jill Buckley serves as Adjunct Assistant Professor in the School of Health Professions at Rutgers University as well as Adjunct Faculty in the Department of Health Technologies at Durham Technical Community College teaching drug safety and pharmacovigilance courses. Jill has worked over 30 years in pharmaceutical industry. For nearly 20 years, Jill has held leadership roles in drug safety and pharmacovigilance at several pharma companies, a CRO, and a consulting firm. Jill gained experience in clinical research and regulatory affairs developing protocols, clinical trial monitoring, regulatory application preparation and FDA interactions. Jill earned Doctor of Pharmacy degree from the University of Michigan.

  • Stephen Gerard Buckley, PharmD

    Stephen Gerard Buckley, PharmD

    • Drug Safety Consultant
    • SGB Safety Consultants LLC, United States

    Dr. Stephen Buckley is an independent drug safety consultant. Prior to this, he was employed at GlaxoSmithKline for 28 years in both drug safety as well as medical affairs/clinical research. While in drug safety, Dr. Buckley represented Global Clinical Safety and Pharmacovigilance efforts having been responsible for aggregate safety reports, safety analyses and leading safety activities for compounds in clinical development. Steve earned both his Bachelors and Doctorate degrees in pharmacy at the University of North Carolina – Chapel Hill.

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