棋牌——协助研究者提升临床试验质量
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临床研究协调员/临床研究护士(CRC)

 

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   Job Qualifications


1. 护理学相关专业本科学历;
2. 有护理相关经验;
3. 英语CET-4及以上,CET-6优先。


1. Bachelors Degree in nursing related major.
2. Minimum 1 year’s nursing related experience.
3. CET-4 at least, CET-6 is preferred.

 

工作地点:全国各省会城市

 

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