Clinical trial site management
Our clinical trial site management services include:
- Site selection
- Feasibility and risk assessments, tailored to country-specific requirements
- Contract and budget management
- Preparation of site documentation
- Ethics Committee and Regulatory documentation submissions
- Patient recruitment and retention
- Training for site staff
- Dedicated, de-centralised CRAs
- Clinical monitoring through every stage of the clinical trial
- Site communication strategy
- Drug accountability
- Transparent reporting
We specialise in rare disease and oncology clinical trials, so are experienced with the unique demands of these complex studies.