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招募临床研究协调员/临床研究护士(CRC)
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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. 招募地点:北京、郑州、哈尔滨、沈阳、呼和浩特、济南、青岛、天津、上海、乌鲁木齐、重庆、厦门、常熟、金华丽水地区、温州、宁波、杭州、汕头、昆明、武汉、长沙、衡阳、常德、岳阳、南昌 |
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