Demo – How a ClinOps Team Achieved 100% of Studies Within Risk
With continuous risk monitoring, this ClinOps team was able to immediately investigate root cause and assign action items to:
- Alert resources at sites with excessive query resolution time
- Task a CRA to follow up with sites missing critical primary and secondary endpoint data
- Target study coordinator retraining for sites with protocol deviations exceeding thresholds
With strong cross-system visualizations, forecasting, alerting and integrated collaboration capabilities, this ClinOps team was able to proactively keep their studies in the green.