Sue Sullivan
About Sue Sullivan
Sue Sullivan is an Associate Director of Statistical Programming at Travere Therapeutics, with a diverse background in statistical programming and clinical research spanning over three decades. Her previous roles include positions at d-Wise, inVentiv Health Clinical, Synteract, Inc., Neurocrine Biosciences, and various research institutions.
Work at Travere Therapeutics
Sue Sullivan has been serving as the Associate Director of Statistical Programming at Travere Therapeutics since 2021. In this role, she oversees statistical programming activities, ensuring the integrity and accuracy of data analysis in clinical trials. Her responsibilities include managing programming teams and collaborating with cross-functional departments to support the development of innovative therapies.
Previous Experience in Statistical Programming
Prior to her current role, Sue Sullivan accumulated extensive experience in statistical programming across various organizations. She worked at d-Wise as a Senior Life Sciences Consultant from 2015 to 2018 and as a Life Sciences Consultant from 2013 to 2015. At Synteract, Inc., she held multiple positions, including Statistical Programmer I-II from 2009 to 2011 and Senior Lead, Statistical Programmer from 2011 to 2012. Additionally, she served as a Senior Statistical Programmer at inVentiv Health Clinical from 2012 to 2013.
Background in Research and Development
Sue Sullivan's career in research and development began at The Scripps Research Institute, where she worked as a Research Associate from 1990 to 1992. She continued her research career at the University of California San Diego, serving as a Research Associate in the Department of Medicine from 1992 to 1997. Following her research roles, she transitioned to Neurocrine Biosciences, where she worked as a Scientist in Pharmacology from 1997 to 2006.
Education and Professional Development
Sue Sullivan earned a Bachelor of Arts degree in Biochemistry/Cell Biology from the University of California, San Diego. She also completed a Professional Certificate in Clinical Trial Design and Management from the same institution. Her educational background provides a strong foundation for her work in statistical programming and clinical research.