职位描述
工作职责 Job Responsibility
(a) Pre-trial Documentation
临床前文档的准备工作
(b) Trial Management: help investigator with trial management, including coordinating the submission of
IRB/EC and Agreement signature process.
试验管理：协助研究者进行试验管理，包括协调申报伦理、研究协议签署等。
(c) Support investigator’s daily work, including:
协助研究者的日常工作，包括：
Labeling, packaging and storing all laboratory specimens before shipment to central lab.
Filling CRF under investigator’s approval.
(d) Subject Management:
受试者管理：
Help investigator to identify and enroll potential study subjects.
Responsible for subjects’ follow-up, including visits arrangement, coordinating laboratory and
obtaining results.
(e) Coordinating CRA’s routine visits.
协调CRA 到site 的例行访视。
(f) Documents Management: Responsible for archiving and maintain trial related documents.
临床试验档案管理：负责该中心的临床试验项目文件整理和归档。
(g) Drug Management: Including research drug accounting, receiving, saving, distributing and calling-back,
and completing related record.
协助完成临床研究药物管理和计数，包括药物的接收、保存、分发、回收和归还，并完成相关记录。
(h) Meeting Supporting: Provide logistic support for initiating meeting and any other investigator meeting.
会议支持：负责各项启动会议、研究者会议的会务安排。
(i) Other daily work delegated by investigator.
研究者指定的其它工作。
任职要求
1. 护理学、药学相关专业大专及以上学历；
2. 英语CET-4及以上。
此项目为期4个月，签4个月的兼职合同或者全职合同，项目结束后调往其他区域。
