? 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 無CTA經(jīng)驗