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岗位职责： • Applies knowledge of Company s policies and procedures • Demonstrates excellent written and oral communication • Demonstrates excellent knowledge of ICH/GCP and relevant local requirements • Displays ability to manage investigative sites to facilitate trial deliverables • Demonstrates ability to escalate issues appropriately • Conducts monitoring to confirm subject safety and data integrity • Describes and demonstrates the principals of IP accountability9. Demonstrates working knowledge of Microsoft Office applications • Demonstrates excellent knowledge of ICH GCP • Identifies scientific misconduct at the site level • Demonstrates working knowledge of Clinical Trial Management Systems, e-TMF, IVRS/IWRS and Electronic Data Capture Platforms • Mentors CRAs new to the position or company • Serves as an observation visit leader • Identifies scientific misconduct at the site level and capability to manage effectively • Reads, writes and speaks fluent English and is fluent in host country language 任职资格的具体描述： 1. 2年以上CRA经验 2. 优秀的英语能力（听说读写），能在全英语环境中工作 3. 有Global经验者优先 4. 有肿瘤科，中枢神经科经验者优先 5. 可以适应长期出差 有意者请速速联系我：Clare.Zhang@FutureStep.com |
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