Phase II-IV Clinical Trials:
Clinical Trial Management and Monitoring

Co-ordination of Investigator Meetings
Investigator meetings coordinated by RCRS are geared toward creating a dynamic environment for the interaction of individuals with a common purpose. These interactive meetings are designed to be both informative and thought provoking, and enable investigators to develop a dialogue with sponsors on best practices for managing the study and gathering clinical trial data. The meetings also include training in key areas including trial protocol, current Good Clinical Practice and study-specific procedures.

A successful investigator meeting helps to build stronger relationships with key target audiences and provides a platform from which to launch enduring materials to broader audiences. From scientific presentations to program management, meeting services, creative design and production, RCRS aims to conduct meetings that are engaging, dynamic and effective.

RCRS utilizes proactive processes for management of diverse investigative sites, including onsite visits to ensure necessary standards for conducting the study, training of site personnel, identifying and offering customized solutions to logistic issues faced at sites, and coordinating resolution of non-compliance issues in a speedy manner. Throughout each clinical trial, the group works closely with sites to upgrade infrastructure to fulfill trial and current regulatory requirements. The RCRS team works closely with investigators to accelerate patient recruitment and ensure patient compliance. RCRS applies real-time site performance metrics that track the progress of studies at each site.