Shelley Dunn
About Shelley Dunn
Shelley Dunn is a Senior Director of Statistical Programming at Travere Therapeutics, with extensive experience in clinical trial processes and statistical analysis. She has held various positions in statistical programming and consulting across multiple organizations, including Synteract, Inc. and d-Wise.
Work at Travere Therapeutics
Shelley Dunn currently serves as Senior Director of Statistical Programming at Travere Therapeutics, a role she has held since 2020. In this position, she oversees statistical programming efforts and contributes to the design and analysis of clinical trials. Dunn has also been the Director of Statistical Programming at Travere Therapeutics since 2017, indicating her long-term commitment to the organization. Her work involves leading programming and validation efforts across various phases of clinical trials, ensuring compliance with industry standards.
Previous Experience at Synteract, Inc.
Dunn has a substantial history with Synteract, Inc., where she held multiple roles over several years. She began as a Programmer/Analyst I in 2000 and progressed to Clinical Data Manager and Clinical Data Coordinator. She served as Manager of Statistical Programming from 2006 to 2008 and later as Sr. Manager from 2008 to 2012. Her final role at Synteract was as Associate Director of Statistical Programming in 2012. Throughout her tenure, she contributed to various clinical trial processes and programming efforts.
Consulting Experience at d-Wise
Shelley Dunn worked at d-Wise as a Life Science Consultant from 2012 to 2013 and later as a Senior Life Science Consultant from 2013 to 2016. In these roles, she provided consulting services to pharmaceutical and biotech companies, focusing on statistical analysis solutions and standards implementation. Her experience at d-Wise allowed her to enhance her expertise in clinical research and contribute to process improvements within the industry.
Educational Background
Dunn holds a Master of Science for Teachers in Mathematics from the University of New Hampshire, which she completed from 1991 to 1993. She also earned two Bachelor's degrees from the University of California, Santa Barbara, in Sociology and in Science Mathematical Sciences with a statistical emphasis, from 1980 to 1985. This educational foundation has equipped her with a strong analytical background, supporting her career in statistical programming and clinical research.
Leadership and Contributions to Clinical Standards
Dunn has demonstrated leadership in the clinical research field by co-leading the ADaM Compliance Sub-Team, which focused on the development and implementation of CDISC standards. Her extensive experience includes leading programming and validation efforts in Phase I-IV clinical trials, showcasing her expertise in clinical trial processes. She has also conducted client assessments regarding standards development in the pharmaceutical and biotech industries, emphasizing her role in advancing industry practices.