Description
The Study Delivery Associate provides administrative and operational support for clinical trial management activities, including study coordination, timelines, risk and quality reviews, training and inspection readiness, global site communications, logistics, vendor and site engagement, biological sample reconciliation, investigational product logistics, clinical systems data entry, document preparation, TMF filing, and process improvement. The role requires a bachelor’s degree or an associate’s degree with four years of clinical execution experience, or a high school diploma/GED with six years of clinical execution experience; life sciences experience and global clinical trial experience are preferred.
