? 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(wú)CTA經(jīng)驗(yàn)