审核修改临床研究协调员撰写的临床研究方案，病例表格等研究文件，保证得到区域和总部相关部门的批准；
Review and revise clinical documents like protocol, case report form, etc, ensure it get approval from country medical director and appropriate central medical head.
在本次讲座中，通过对实例的讲解，参与者能够了解到临床数据如何在数据管理者、临床研究协调员、研究者和监察员间传递。
Through an example trial in this speaking series, participants will observe how clinical data flows between data managers, CRCs, investigators and monitors.
临床研究者、协调员、临床监察员以及数据管理员等临床试验中的各种角色都能通过电子数据采集享受到特有的便利。
Researchers of various roles involved in clinical trials, such as investigators, study coordinators, site monitors and data managers, can enjoy unique benefits offered by EDC.
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