Brittany Groner
About Brittany Groner
Brittany Groner serves as the Associate Director at BridgeBio, where she has worked since 2020. She possesses extensive experience in managing clinical studies across various phases, particularly in rare diseases, oncology, and pulmonary conditions.
Work at BridgeBio
Brittany Groner has been serving as the Associate Director at BridgeBio since 2020. In this role, she is responsible for overseeing the management of clinical studies, ensuring adherence to regulatory guidelines and Good Clinical Practices. Her responsibilities include leading cross-functional study teams, managing study budgets, and developing quality control processes. Groner plays a key role in the development and compliance of Standard Operating Procedures, contributing to the overall efficiency and effectiveness of clinical activities within the organization.
Previous Experience in Clinical Research
Prior to her current position, Brittany Groner held various roles in clinical research. She worked at Premier Research as a Senior Clinical Research Associate for three months in 2018 and later served as Clinical Manager 1 and Clinical Manager 2 at the same organization from 2018 to 2020. Groner also gained experience at PAREXEL, where she worked as a Clinical Research Associate and Clinical Monitoring Associate II from 2014 to 2016. Additionally, she was employed at PRA International as an In-House Clinical Research Associate from 2011 to 2014.
Education and Expertise
Brittany Groner earned her Bachelor of Science (B.S.) degree in Environmental Science from the University of North Carolina Wilmington, completing her studies from 2007 to 2011. Her educational background supports her extensive experience in managing clinical studies across various phases, with a focus on rare diseases, oncology, and pulmonary conditions. Groner's expertise includes developing study plans, coordinating scientific communication, and ensuring compliance with clinical and regulatory standards.
Clinical Study Management Skills
Brittany Groner has developed a robust skill set in managing clinical studies throughout her career. She is adept at overseeing study budgets, including forecasting and internal reporting, which ensures financial accountability. Groner leads cross-functional teams to execute study plans and is responsible for organizing and presenting at investigator meetings. Her role also involves coordinating the development of abstracts, presentations, and manuscripts for clinical studies, enhancing scientific communication and dissemination.