Site Monitoring and Oversight Service

Our team of clinical research associates (CRAs) act as our clients’ ambassadors on site. They ensure smooth operational trial delivery by engaging, motivating and supporting the trial sites from set-up and implementation all the way through to trial close out. Monitoring and site oversight is one of the most resource-intensive aspects of a clinical trial. It is essential it is done to a high standard to ensure patient safety, data integrity and regulatory compliance. We offer a cost-effective solution to managing trial sites.

Our services include site identification, set-up, monitoring, oversight, and close-out ensuring strict adherence to ICH-GCP and regulatory requirements.

We have a large network of CRAs and routinely offer monitoring services in Europe and USA and have a growing global footprint. Our CRAs go the extra mile to ensure all trial-associated staff fully understand the trial protocol and prioritise the needs of the patient throughout. Our team has significant clinical trials experience, gained over many years across all trial phases and therapeutic areas.

Our flexible approach to monitoring incorporates both on-site and remote monitoring activities to ensure trial delivery to the highest quality standards.


Our Monitoring and Oversight Service specialises in supporting oncology and orphan diseases. We provide you with an extensive network of trusted site monitors to identify, set-up and oversee investigator sites on behalf of clients:

  • Act as study ambassadors
  • Engage, motivate and support sites
  • Deliver to their commitments
  • Cost-effective solution to managing study sites
  • Access to a large and growing pool of experienced monitors across core markets