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William C. Tubbs has a strong background in regulatory affairs and quality assurance, with over 20 years of experience in the industry. William C. is currently serving as the Head of Regulatory Affairs at Visterra Inc. since January 2019. Prior to that, they worked at Shire as a Director from September 2015 to January 2019. Before joining Shire, Tubbs was the Director of Regulatory Affairs and Quality Assurance at Promedior, Inc., where they focused on the clinical development of recombinant protein for myelofibrosis and idiopathic pulmonary fibrosis. William C. also held positions as Associate Director Regulatory Affairs at AVEO Oncology, Millennium Pharmaceuticals, and AVANT Immunotherapeutics, and as a Senior Regulatory Affairs Specialist at BioPure Corporation. Tubbs began their career as a Regulatory Affairs Specialist at Massachusetts Public Health Biologic Laboratories and later gained valuable experience as a Quality Assurance Compliance Specialist at Genzyme.

William C. Tubbs has a Bachelor of Arts (B.A.) degree in Philosophy from Birmingham-Southern College. William C. also pursued studies in Philosophy of Religion at the Boston University Graduate School of Arts and Sciences. Additionally, they obtained a Master of Theological Studies degree from the Boston University School of Theology. In 2005, Tubbs earned certification as a Regulatory Affairs Certified from the Regulatory Affairs Professionals Society (RAPS).