Clinical Research: Clinical Monitoring

With extensive experience, we are firmly focused on delivering projects within a controlled process and structure that is proven to deliver reliable results. At PRN we conduct both formal on-site monitoring as well as remote and electronic data monitoring.

Clinical Monitoring Experience

PRN Clinical Research Associates (CRAs) are experienced and well supported via our ‘hands on’ management approach.
We have a comprehensive co-monitoring policy to continually review the CRA’s monitoring activities at sites.

Fast Study Site Set Up

We provide a larger team for the set-up period – whilst making sure the sites are allocated their Clinical Research Associate from study start-up to maintain continuity and good site relationships.

Specialist Experience in Early Phase Monitoring

We have CRAs experienced in Phase I studies who will work with your Study Leaders, enabling you to manage the set-up and reporting of multiple Phase I studies whilst controlling headcount and budget.

Non-interventional Studies – experienced teams and separate procedures

In addition to our experience in phase I-IV clinical research studies we have teams with specialist expertise in the management of non interventional studies e.g. late phase observational studies and registry studies. These types of studies require a very different methodology and progress can be unnecessarily hindered by a traditional clinical approach. PRN can provide you with feasibility and study design as well as project managing the set-up and ongoing data monitoring phases of such studies with experienced data managers and statisticians providing the data analysis and final reporting.