Data Coordinating Center for Multi-Site Investigator-Initiated Clinical Trials (Collaborative U24 Clinical Trial Required)
This Notice of Funding Opportunity (NOFO) supports applications for a collaborating Data Coordinating Center (DCC) for investigator-initiated multi-site clinical trials including efficacy, comparative effectiveness, pragmatic and/or implementation research clinical trials. Trials
About this program
The Data Coordinating Center (DCC) grant supports the coordination and management of multi-site clinical trials initiated by investigators. It aims to enhance the efficiency and effectiveness of clinical research by providing centralized data management, statistical analysis, and logistical support. The DCC will work with various clinical sites to ensure that data collection and reporting are standardized and compliant with regulatory requirements. This grant is intended for institutions and organizations that have the capacity to manage large-scale clinical trials. Eligible applicants must demonstrate experience in coordinating multi-site studies and have the necessary infrastructure to support data management and analysis. The DCC will facilitate collaboration among investigators, streamline processes, and ensure that trials are conducted in accordance with best practices and ethical standards.
Eligibility
Eligible applicants include institutions and organizations with experience in managing multi-site clinical trials.