长沙招聘

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.

泰格医药是行业领先的一体化生物医药研发服务平台，为全球制药和医疗器械行业提供跨越全周期的临床研究创新解决方案。通过全面的服务体系和***的质量标准，我们助力生物医药产业提升研发效率、降低研发风险，确保研究项目高质量交付，加速医药产品市场化进程，履行对行业和患者的承诺。同时，我们也通过覆盖各领域的80多家子公司，打造赋能全产业链的创新生态，推动医疗产业创新和发展。作为全球化的研发平台，泰格医药在全球布局170多个办事处和研发基地，拥有超过8600人的专业团队，覆盖5大洲的51个国家，致力于解决最具挑战的全球健康问题，满足患者的未尽医疗需求，创造社会价值，造福人类健康。