Обязанности и достижения:
Identify, select, initiate, and close-out appropriate investigational sites for clinical studies. Monitor those sites in order to ensure that studies are carried out according to the study protocol, SOPs, applicable regulations and the principles of ICH-GCP Depending upon experience, become involved, when required, in other areas of study management and staff training and contribute to the review of systems and procedures as appropriate. Provide a benchmark of monitoring competence to inexperienced/less experienced colleagues.