• To administer, maintain and coordinate the logistical aspects of the clinical trials according to GCP and SOPs
• Work side-by-side with CRA and assisting in some of their tasks
• Prepare and maintenance of the various documents and CRFs for the study
• Perform liaison activities with the Independent Ethics Committees
• Be the central contact and support between the contract laboratory, study team and study site
• Provide logistical support for the clinical trial
• Provide agenda, minutes and action points for meetings
• Assist in managing the site budget activities

可接受master Fresh graduate 无CTA经验