This Clinical Trial Agreement template is designed to facilitate clear, compliant, and efficient collaboration between research sponsors and research sites engaged in clinical trials. Provided by centerwatch.com, this resource outlines essential legal, regulatory, and operational terms required for conducting clinical studies, including roles and responsibilities, compensation, confidentiality, data ownership, regulatory compliance, and publication rights. We offering this standardized framework with the goal of helping both sponsors and institutions navigate the complexities of clinical research agreements, ensuring alignment with industry best practices and regulatory expectations.
Clinical Trial Agreement Template
Updated on November 5, 2025
Originally published on July 1, 2025

