Passionate about supporting sites and patients
A clinical trial has many complex, moving parts and each must be monitored to protect the safety of study participants while keeping the study running according to protocol and regulatory requirements.
Streamlining strategy to mitigate risks and drive data integrity in clinical trial monitoring
We take a risked-based approach to developing and executing the project monitoring strategy. To ensure quality execution, patient safety and data integrity, we use comprehensive dashboards customized to the specific risks of each trial.
Orchestrated by the Clinical Trial Manager, our highly skilled Central Monitors (CTs) and clinical research associates (CRAs) collaborate closely and work in sync along with our Risk Managers and RBM subject matter experts to resolve concerns swiftly so that patients stay safe, studies stay on schedule and results remain robust.
- Issues are detected 20% faster than by traditional monitoring methods
- 40% of queries and protocol deviations are detected by our CMs so that CRAs can focus on taking corrective actions with sites