Clinical Monitoring

ORION’s CRAs are based either regionally or in one of our five offices. This approach enables us to monitor in more than 20 countries of the world in a flexible and cost-effective manner.

As you would expect, our monitors are fully trained in GCP, the therapeutic area and the specifics of your study protocol.

However, we also expect our CRAs to pro-actively manage their investigative sites.

Working closely with their study Project Manager, the monitors develop individual management plans for each of their centres – this includes a site-specific recruitment plan based on feasibility work. Our CRAs will also establish productive relationships with the Principal Investigator and other key players; they are responsible for ensuring that the activities of laboratories, pharmacists and other providers are fully integrated.

In summary, we encourage our CRAs to act as Project Managers of their investigative sites.