Services > Site Support
The MRN can provide specialist clinical and contract research nurses that are placed directly in the research site. These additional resources will not only manage the patients but will also perform day-to-day administrative burdens thus releasing investigators for patient care and other principle investigator activities.
Tasks performed by the nurse include:
• Study site co-ordination
• Site documentation management
• Integration and communication with other departments
• Patient screening and recruitment
• Drug administration
• Paper / eCRF completion
• Query management
Please call or complete an on-line query form to speak to the MRN about how we can support your clinical trial needs.
Realistic and Accurate Feasibility Data
The MRN can place clinical research nurses into clinics and GP surgeries & practises to trawl through patient notes and files.
The outcome is that we can identify realistic recruitment rates for clinical trials, thus providing our sponsors with more accurate data for trial planning and feasibility. This can be particularly useful when working with a site for the first time or where research naive sites are to be included in a trial.
