Why would we utilise the CPR to project manage studies when the clinical site can handle the whole package?
It is not mandatory that the CPR handle the project management of studies, we are able to provide a cost effective quality service in any of our core areas. We have, however, found that companies with significant project pipelines often utilise the CPR for project management purposes for the following reasons: • Ease the logistical burden of managing several trials simultaneously • Ability to place all non site specific activities with one provider (ie. protocol review, CRF design, initiation, monitoring, data management, bio-analysis, pharmacokinetic and statistical analysis and report writing with a single provider).
