Our Services
 Home > Our_Services > Site Management
Site Management and Clinical Monitoring

The comprehensive services of the DCRI include unique site management and clinical monitoring capabilities. Our Site Management staff are clinically knowledgeable, which means their methods are not only innovative but also in tune with the needs of clients, patients, and investigators alike. The results are streamlined, efficient site services that hasten recruitment and study execution.

Our experienced Site Management teams have coordinated some of the most significant and groundbreaking trials of the past decade. This hard-won track record provides DCRI Site Management with unparalleled tools and processes that have withstood the test of research ranging from small, regional studies to truly global megatrials. Our database of proven study sites is an invaluable resource, giving sponsors confidence that our investigators and site personnel can enroll and follow patients with speed and efficiency.

Beyond the usual management services, including both on-site and in-house monitoring, coordination of monitors, and data collection, DCRI Site Management offers a complete portfolio of capabilities reflecting our unique blend of academic, clinical, and operational acumen.

Leader and contact: Bunny Dunohue

   

From cutting-edge electronic data capture to a dedicated Safety Surveillance department, no aspect of study site coordination is beyond our abilities.

• Investigator qualification/selection and site recruitment
• Investigative site start-up and training
• Facilitation of clinical trial enrollment
• Ensuring site regulatory compliance
• CRF completion, data collection and query resolution
• Expedited adverse-event reporting

Site Map Contact Us Links Help Terms of Use © 2003-2008 Duke Clinical Research Institute.