- 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