Tieng Doan

Tieng Doan is an accomplished regulatory operations professional with extensive experience in the pharmaceutical industry. Currently serving as Sr. Manager of Regulatory Operations at Intercept Pharmaceuticals since February 2020, Tieng Doan manages global regulatory operations and collaborates with interdisciplinary teams to facilitate submission components. Previous roles include Independent Consultant at Quality eDocs, where Tieng Doan provided support for regulatory affairs and quality assurance across various submission types, and Consultant at Tocagen Inc. and Intercept Pharmaceuticals, focusing on electronic document management and quality checks for regulatory submissions. Tieng Doan's career has also included positions with Ardea Biosciences, Lithera, Inc., Amylin Pharmaceuticals, Inc., and Aguoron/Pfizer Inc., accumulating a wealth of expertise in regulatory processes, document publishing, and compliance across a wide array of product submissions.