Jack Verga
About Jack Verga
Jack Verga serves as the Associate Director at BridgeBio in Raleigh, North Carolina, where he has worked since 2021. With over 15 years of experience in the Clinical Research Industry, he specializes in Clinical Data Management and Project Management across various therapeutic areas.
Work at BridgeBio
Jack Verga has been serving as the Associate Director at BridgeBio since 2021. He is based in Raleigh, North Carolina, where he contributes to various projects within the organization. His role involves overseeing clinical data management and ensuring operational efficiency across sponsor portfolios.
Previous Experience in Clinical Data Management
Before joining BridgeBio, Jack Verga held several positions in the clinical research industry. He worked at PRA Health Sciences as a Manager in Clinical Data Management from 2018 to 2019. Prior to that, he served as a Trial Manager in the Strategic Solutions Division of PRA Health Sciences from 2015 to 2018. His career also includes roles at Syneos Health Clinical Solutions and PPD, where he gained extensive experience in clinical data management.
Educational Background
Jack Verga studied at Long Island University, where he earned a Bachelor of Science in Biology Education and Psychology from 1997 to 2000. He furthered his education at the same institution, obtaining a Master of Science in Biology and Behavioral Ecology from 2000 to 2002. This academic foundation supports his extensive career in clinical research.
Therapeutic Area Expertise
Jack Verga has developed therapeutic area expertise in several fields, including Oncology, Cardiovascular Disease, Neurology, and Infectious Disease. His experience spans various phases of clinical trials, specifically phases 1, 2, and 3, from both contract research organization (CRO) and sponsor perspectives.
Contributions to Clinical Research
Jack Verga has over 15 years of experience in the clinical research industry, focusing on clinical data management, project management, and operational oversight. He actively participates as a subject matter expert during regulatory inspections and vendor audits. Additionally, he contributes to the development of Standard Operating Procedures (SOPs) and provides training on data management systems.