All our research nurses and co-ordinators are selected according to the individual visit, site or trial requirements. For example, where clinical sites have little or no clinical trial experience, we will ensure the individual placed is very experienced and can not only support the site, but also train and mentor staff on trial requirements.
|All our nurses are fully trained in ICH GCP before they are placed on site and any study specific training is agreed with the Sponsor upfront. This training can be done on-site, face-to-face or via our training portal MRN-TEC.|
MRN also has experience of running locally-based specialist multi-lingual study teams who can travel around global sites to undertake specialized study site activities such as medical device management or complex drug titration.
We have experience of placing whole teams of nurses into limited experience sites or sites that would otherwise have been rejected on trials and have ensured that they performed as well as, or even better than, more experienced sites.