Clinical Study Monitoring
We minimize the number of protocols assigned to each CRA, allowing them to develop protocol expertise and share lessons learned across sites, thereby promoting positive site relationships and quality data review.
Our robust monitoring activities are supported by implementing techniques such as:
- Addressing queries remotely, prior to site visits
- Reviewing site data trends and issues (pre-visit) to enhance productivity during site visits
- Ongoing collaboration with data management
- Implementing risk-based monitoring strategies when appropriate
As part of our ongoing commitment to attracting and retaining the industry’s best CRAs, we employ a dedicated in-house CRA mentor who provides new learning opportunities to our team members, continuously expanding their industry, technology, and oncology expertise.