Carrie Story
About Carrie Story
Carrie Story serves as the Associate Director of Data Management at Travere Therapeutics, a position she has held since 2021. With extensive experience in data management across various pharmaceutical companies, she has contributed to the field for over a decade.
Work at Travere Therapeutics
Carrie Story has been serving as the Associate Director of Data Management at Travere Therapeutics since 2021. In this role, she oversees data management processes and ensures the integrity and quality of clinical trial data. Her tenure at Travere Therapeutics has spanned three years, during which she has contributed to the company's mission of developing innovative therapies for rare diseases. Prior to her current position, she worked as a Principal Data Manager at the same organization from 2019 to 2021.
Previous Experience in Data Management
Before joining Travere Therapeutics, Carrie Story held the position of Manager of Data Management at Acadia Pharmaceuticals Inc. from 2013 to 2019. During her six years at Acadia, she managed data operations and supported various clinical projects. Additionally, she worked at Baxter Healthcare as a Senior Clinical Data Associate for one year in 2008-2009 and at Neurocrine Biosciences for four months in 2007. Her experience also includes a three-year tenure at Elan Pharmaceuticals as a Senior Clinical Data Associate from 2003 to 2006.
Career Development in the Pharmaceutical Industry
Carrie Story's career in the pharmaceutical industry began with her role as a Senior Clinical Data Associate at Elan Pharmaceuticals. She then transitioned to Allergan, where she worked as a Principal from 2009 to 2013. Her diverse experience across multiple companies has equipped her with extensive knowledge in data management and clinical operations, contributing to her advancement to managerial roles in the field.
Location and Professional Background
Carrie Story is based in San Diego County, California. Her professional background includes significant experience in data management within the pharmaceutical and biotechnology sectors. She has worked in various capacities that have allowed her to develop a comprehensive understanding of clinical data processes and regulatory requirements.