When it comes to successful project execution, collaboration with dependable sites are key for on-time enrollment, data collection and quality, and patient safety. Our dedicated Site Relations team is responsible for:
- New site identification and feasibility
- Site selection and qualification
- Site regulatory support & TMF management
- Essential document collection, review and processing
- Investigator relationship management and maintenance
- Ongoing site surveys to find areas of improvements
- Assist with obtaining approval from local Ethics Committees and Institutional Review Boards
- Communication with investigator sites
- Mass mailings and newsletters
We have generated a robust database of high-performing, dependable sites based on therapeutic area, We have also gathered past site performance data that enables us to predict realistic site activity and data quality for your trial.
