Our vast experience working with sponsors and CROs has led to the development of a novel clinical monitoring services group providing an unparalleled level of quality, commitment and execution.
The advantages of Neozene clinical trial monitoring teams are clear:
Our employment relationships vest monitors in the efficiency, quality and success of projects. Our monitors are not continually pondering better opportunities and leaving your project – they are the best compensated and most experienced clinical research professionals and are committed to your protocol from initiation to closure.
A Project Manager will compose a team most appropriate for the protocol, taking into account the monitors’ therapeutic experience, availability and region. Above all, you are assured a superior Clinical Trial Monitoring experience not possible with a traditional CRO.
Our experienced monitors are responsible for monitoring the activities of investigational sites throughout a clinical study. Monitoring responsibilities include pre study, initiation, interim monitoring and closeout visits.
Routine Monitoring Services include: