Efficient site management is essential for an effective trial and rapid collection of accurate results.
Our CRAs are highly-trained and available 24/7. They are adept at building long-term partnerships with investigators and supporting efficient trial recruitment, as well as ensuring proper data quality and consistency.
Throughout the study, our team provides support in areas, including:
- site personnel training and education
- study drug and non-drug supplies logistics
- tracking regulatory document revisions
- tracking protocol deviations
- tracking subject status within the trial