Site Management & Monitoring

• Site in-service training
• Coordination of site contracts and payments
• Enrolment and retention strategies
• Manage and monitor national and international clinical sites
• Ensure rights and well-being of human subjects are protected
• Ensure trial data are accurate, complete and verifiable from source documents
• Ensure trials are conducted in accordance with local and international laws and applicable regulations and guidelines
• Provide feedback to site including overall site conduct, deficiencies and required actions
• Monitor site performance throughout the trial
• Query resolution
• Maintenance of central study files