Description
The Study Delivery Associate provides administrative and operational support for clinical trial management activities, including study coordination, clinical systems and data management, document preparation, TMF filing, training and inspection readiness, vendor and site engagement, and investigational product logistics. 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 or medically related experience is preferred.
