Ref #: 25949

Employment type: Permanent - Full-Time

Location: China-Shanghai


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