LEAD PHARMACOKINETICIST
US Food and Drug Administration
Silver Spring, Maryland
Dr. Heather Boyce serves as a Lead Pharmacokineticist for the Modified Release Oral Drug Products Team in the Division of Therapeutic Performance II (DTPII), Office of Research and Standards (ORS), Office of Generic Drugs, Center for Drug Evaluation and Research at the Food and Drug Administration in White Oak, MD.
Dr. Boyce brings 13 years of experience in the pharmaceutical industry with expertise in good manufacturing processes (GMP), pharmaceutical manufacturing and product development, clinical trial design and analysis, clinical pharmacology, and Title 21 Code of Federal Regulations (CFR) interpretation and compliance.
Prior to her current role, Dr. Boyce served as Acting Team Lead for the Immediate Release Oral Drug Products Team in DTPII. In both roles, Dr. Boyce leads the development of product specific guidance (PSG) for oral drug products.
Dr. Boyce received her PhD in Pharmaceutical Sciences at the University of Maryland, Baltimore, School of Pharmacy where her research focused on excipient properties and formulation design of pharmaceutical drug products. She received her Bachelor of Science degree in chemistry with a minor in mathematics from Temple University of Philadelphia, PA.
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