Clinical research infrastructure development

Research site assessment and preparatory study development

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
QCR has many years of experience training research coordinators and clinical monitors. We have performed domestic and international on-site training sessions for study coordinators, principal investigators, and laboratory personnel on study conduct issues (e.g., Case Report Form completion, safety reporting, GCP compliance, FDA audits). We have years of experience preparing monitors to work in the field, and we also have performed extensive on-site training. We can provide tools such as working procedures, checklists, and Study Reference Manuals to assist both site personnel and monitors to ensure that they are producing quality work.

Access to well-trained and experienced investigators