Clinical Trial Coordinator

The Clinical Trial Coordinator will coordinate, oversee, and complete functions for assigned trial activities, ensuring tasks are performed on time, within budget, and to a high-quality standard. This role involves proactively communicating risks, providing system support, and ensuring system databases are current. Responsibilities include performing administrative tasks such as processing documents, conducting reviews, and distributing communications. The coordinator will also analyze and reconcile study metrics, assist with clarification of findings, and help coordinate study materials and supplies. Maintaining knowledge of SOPs and regulatory guidelines, supporting scheduling, reviewing local regulatory documents, and assisting with study-specific documentation and systems are also key duties. The role includes maintaining vendor trackers, supporting regulatory submissions, preparing compliance review packages, and collaborating with internal departments and teammates to meet project deadlines and address site issues.