Our highly experienced and skilled site monitors and managers provide the following services to sponsors and independent investigators who requiring support to oversee clinical projects:

• Conduct onsite and remote monitoring visits in according with the protocol, monitoring plan and study SOPs
• 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 and reported trial data are accurate, complete and verifiable from source documents
• Ensure trials are conducted in accordance with the local and international laws, applicable regulations and guidelines governing the conduct of clinical trials
• Provide appropriate verbal and written feedback to site, listing overall site performance, deficiencies and corrective action required
• Monitor site performance throughout the trial and communicate any issues as appropriate
• Serve as the main line of contact between the sponsor and the investigator
• Query resolution
• Maintaining central study files