ACCOUNTABILITIES
1、To administer, maintain and coordinate the logistical aspects of the clinical trials according to GCP and SOPs
2、Work side-by-side with CRA and assisting in some of their tasks
3、Prepare and maintenance of the various documents and CRFs for the study
4、Perform liaison activities with the Independent Ethics Committees
5、Be the central contact and support between the contract laboratory, study team and study site
6、Provide logistical support for the clinical trial
7、Provide agenda, minutes and action points for meetings
8、Assist in managing the site budget activities
QUALIFICATIONS, EXPERIENCE & SKILLS
1、Either relevant work experience or High School Diploma (or equivalent)
2、Research or health care related academic or work experience preferable
3、Good organizational skills, ability to manage multiple tasks and meticulous attention to detail
4、Good written and verbal communication skills
5、Good written and spoken English
6、Computer literacy: e.g. Microsoft Word, Excel, PowerPoint, Outlook
职位福利：节日福利、五险一金、交通补助、餐补