Our clinical monitoring teams are built to deliver fast, efficient investigator site support and data oversight for your study. Innovate requires our CRAs to demonstrate proficiency in site monitoring before allocated to a study. Our monitoring services include comprehensive monitoring plans, support for 100% source document verification or risk-based monitoring strategies, identifying and escalating adverse event (AE) issues, routine monitoring, site initiation, interim, and close-out visits, and on-going formal training programs.
Our CRAs conduct on-site monitoring visits throughout the study to:
- Oversee data collection
- Review source documentation and case report forms
- Ensure regulatory compliance
- Resolve data queries
- Conduct interim analyses as requested by clients