職位描述
工作職責 Job Responsibility
(a) Pre-trial Documentation
臨床前文檔的準備工作
(b) Trial Management: help investigator with trial management, including coordinating the submission of
IRB/EC and Agreement signature process.
試驗管理：協(xié)助研究者進行試驗管理，包括協(xié)調(diào)申報倫理、研究協(xié)議簽署等。
(c) Support investigator’s daily work, including:
協(xié)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:
受試者管理：
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.
協(xié)調(diào)CRA 到site 的例行訪視。
(f) Documents Management: Responsible for archiving and maintain trial related documents.
臨床試驗檔案管理：負責該中心的臨床試驗項目文件整理和歸檔。
(g) Drug Management: Including research drug accounting, receiving, saving, distributing and calling-back,
and completing related record.
協(xié)助完成臨床研究藥物管理和計數(shù)，包括藥物的接收、保存、分發(fā)、回收和歸還，并完成相關(guān)記錄。
(h) Meeting Supporting: Provide logistic support for initiating meeting and any other investigator meeting.
會議支持：負責各項啟動會議、研究者會議的會務(wù)安排。
(i) Other daily work delegated by investigator.
研究者指定的其它工作。
任職要求
1. 護理學(xué)、藥學(xué)相關(guān)專業(yè)大專及以上學(xué)歷；
2. 英語CET-4及以上。
此項目為期4個月，簽4個月的兼職合同或者全職合同，項目結(jié)束后調(diào)往其他區(qū)域。
