鑱蜂綅鎻忚堪
宸ヤ綔鑱疯铂 Job Responsibility
(a) Pre-trial Documentation
鑷ㄥ簥鍓嶆枃妾旂殑婧栧倷宸ヤ綔
(b) Trial Management: help investigator with trial management, including coordinating the submission of
IRB/EC and Agreement signature process.
瑭﹂绠＄悊锛氬崝鍔╃爺绌惰€呴€茶瑭﹂绠＄悊锛屽寘鎷崝瑾跨敵鍫卞€悊銆佺爺绌跺崝璀扮敖缃茬瓑銆�
(c) Support investigator鈥檚 daily work, including:
鍗斿姪鐮旂┒鑰呯殑鏃ュ父宸ヤ綔锛屽寘鎷細
Labeling, packaging and storing all laboratory specimens before shipment to central lab.
Filling CRF under investigator鈥檚 approval.
(d) Subject Management:
鍙楄│鑰呯鐞嗭細
Help investigator to identify and enroll potential study subjects.
Responsible for subjects鈥� follow-up, including visits arrangement, coordinating laboratory and
obtaining results.
(e) Coordinating CRA鈥檚 routine visits.
鍗旇CRA 鍒皊ite 鐨勪緥琛岃í瑕栥€�
(f) Documents Management: Responsible for archiving and maintain trial related documents.
鑷ㄥ簥瑭﹂妾旀绠＄悊锛氳矤璨┎涓績鐨勮嚚搴婅│椹楅爡鐩枃浠舵暣鐞嗗拰姝告獢銆�
(g) Drug Management: Including research drug accounting, receiving, saving, distributing and calling-back,
and completing related record.
鍗斿姪瀹屾垚鑷ㄥ簥鐮旂┒钘ョ墿绠＄悊鍜岃▓鏁革紝鍖呮嫭钘ョ墿鐨勬帴鏀躲€佷繚瀛樸€佸垎鐧笺€佸洖鏀跺拰姝搁倓锛屽苟瀹屾垚鐩搁棞瑷橀寗銆�
(h) Meeting Supporting: Provide logistic support for initiating meeting and any other investigator meeting.
鏈冭鏀寔锛氳矤璨悇闋呭暉鍕曟渻璀般€佺爺绌惰€呮渻璀扮殑鏈冨嫏瀹夋帓銆�
(i) Other daily work delegated by investigator.
鐮旂┒鑰呮寚瀹氱殑鍏跺畠宸ヤ綔銆�
浠昏伔瑕佹眰
Job Qualifications
1. 璀风悊瀛哥浉闂滃皥妤湰绉戝姝�
2. 鏈夎鐞嗙浉闂滅稉椹�
3. 鑻辫獮CET-4鍙婁互涓婏紝CET-6鍎厛
1. Bachelors Degree in nursing related major.
2. Minimum 1 year鈥檚 nursing related experience.
3. CET-4 at least, CET-6 is preferred.
