Training consultation and support of Study Site Coordinators /Research Nurses on clinical studies
Providing nonoperational site support to ensure progress of clinical study and to ensure that it is conducted recorded and reported in accordance with the protocol standard operating procedures (SOPs) ICH GCP and the applicable regulatory requirement(s)
Notifying Study Monitor / Team on any site issues that are detected in contact with the clinical center and are relevant for them
Establishing and maintaining relationships with Study Site Coordinators and Investigators to optimize performance of clinical study
Assistance in development of recruitment strategies and tracking of recruitment or patient retention activities at the site
Qualifications :
Bachelor or Master of Science degree or equivalent (preferably in medical field i.e. medical nurse)
Experience as a Clinical site manager Study nurse or study site coordinator
Excellent organisation skills with attention to detail
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