Clinical research infrastructure development

Research site assessment and preparatory study developmentTo ensure a successfully conducted trial, it is important to assess the technical capacity and recruitment capability of the site, as well as the community and political support, prior to initiating the trial. This is particularly important for large scale, community-based trials. QCR has extensive experience in conducting these assessments, including the design of preparatory epidemiologic studies needed to assess the feasibility of conducting clinical trials.

Strategic consulting

Project management for research site coordination and oversight

Liaison with industry, government and other institutions

Safety monitoring

Clinical monitoring

Development of research plans and reports including proposals, timelines, protocols, consent forms, CRFs, SOPs

Medical writing

Preparation of presentations to IRBs, DSMBs, FDA, and other international institutions

Training for research coordinators and monitors

Access to well-trained and experienced investigators