Effective site management significantly improves clinical trial outcomes, especially in rare and orphan diseases. Well-trained clinical research associates (CRAs) are critical because they ensure smooth operations from data quality to protocol compliance and efficient site operations.
Many CRA strategies exist; read the white paper to learn about:
- Methods for effective site management
- Developing a framework for adaptive monitoring
- Strategies for real-time issue resolution, with special considerations for neurodevelopmental and rare condition trials.
