Tess Franco

Associate Director, Regulatory Operations at Xencor

Tess Franco has a diverse and extensive work experience in the field of regulatory operations. Tess started their career as a Manager of Regulatory Operations at Isis Pharmaceuticals in 2001 and worked there until 2004. Tess then joined MediciNova, Inc. as a Manager of Regulatory Affairs, where they oversaw document management and publishing systems. Tess also played a key role in establishing submission and publishing processes for regulatory submissions. Tess worked at MediciNova from 2004 to 2008. After that, they worked as a Manager of Regulatory Affairs at Amylin Pharmaceuticals from 2008 to 2009. Tess then took on consultancy roles at Halozyme Therapeutics, Inc., eSubmissions Solutions, and Ardea Biosciences. In 2013, they joined Samumed LLC as a Senior Manager of Regulatory Operations, where they were responsible for identifying and recommending best industry practices for documentation format and coordinating document numbering and index systems. Tess worked there until 2014 when they joined Intercept Pharmaceuticals as a Manager of Regulatory Operations. Most recently, in 2016, Tess started working at Xencor as an Associate Director of Regulatory Operations.

From 1986 to 1991, Tess Franco attended Arizona State University. The information does not specify a specific degree or field of study.

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