Monitoring clinical trial site operations is key to running a smooth clinical trial that delivers results. We offer our Sponsors flexible approaches to site monitoring, from full-service monitoring to centralized and risk-based monitoring to meet your needs.
Our Clinical Research Associates (CRAs) are an extension of our Sponsors and work directly with sites to meet patient recruitment and study execution goals. With the ability to assign office-based or regional CRAs to your project, we take an approach that is the right fit for your clinical program, focusing on data quality improvement and accelerated database lock.
Study integrity and subject safety are of utmost importance to our team. Nutrasource’s CRAs ensure the highest quality data through the duration of the clinical project, from site qualification through close-out. Throughout the process, we pay specific attention to patient eligibility, protocol adherence and implementation, adverse event management and reporting, clinical regulatory affairs/document maintenance and data management (collection, data entry, and overall accuracy).
Learn how we can help you effectively manage your site operations that meets your needs and project goals.