Market Access and Government Affairs Executive Joins NDA Partners as Expert Consultant


Prior to joining NDA Partners, Dr. Schoonmaker served as Senior Vice President with Cepheid, a leading molecular diagnostics company, where she built and led the Government Affairs and Market Access function. Her primary responsibilities were to develop and implement global strategic reimbursement plans for the company’s molecular diagnostic tests, working with professional associations, federal agencies, and legislative offices on regulatory, reimbursement and disease-specific policies for molecular testing to facilitate the integration of beneficial new technologies into clinical testing. Prior to joining Cepheid, she was a Specialist in Genetics for the Congressional Research Service (CRS), a division of the Library of Congress, and regulatory policy analyst and reviewer of diagnostic tests in the Office of In Vitro Diagnostics (OIVD) at FDA. She also spent 11 years with the National Institute of Aging/National Institutes of Health in the Immunology Laboratory as a Biologist in an earlier role.

Dr. Schoonmaker holds a PhD in Health Services Research, Genetic and Public Policy from The Johns Hopkins University School of Hygiene and Public Health and a bachelor’s degree in biology from Goucher College.

About NDA Partners

NDA Partners, a ProPharma company, is a life sciences management consulting and contract development organization focused on providing product development and regulatory services to the pharmaceutical, biotechnology, and medical device industries worldwide. The highly experienced Expert Consultants in NDA Partners include three former FDA Center Directors; the former Chief Executive Officer and Chief Science Officer at the United States Pharmacopeial Convention (USP); an international team of more than 100 former pharmaceutical industry and regulatory agency senior executives; and an extensive roster of highly proficient experts in specialized areas including nonclinical development, toxicology, pharmacokinetics, CMC, medical device design control and quality systems, clinical development, regulatory submissions, and development program management. Services include product development and regulatory strategy, product development program design and management, expert consulting, functional teams, project-based solutions, and clinical trial design and management.

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Eric Fish, Vice President & General Manager
Office: 540-738-2550
[email protected]

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Eric Fish, NDA Partners, A ProPharma Company, 540-728-2550, [email protected], www.ndapartners.com 

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