Chengdu Kanghong Pharmaceutical Group Co.,Ltd.
临床监查员(CRA)(J10899)
Skills
2 months ago
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Important information
Contract type:
Permanent
Location:
Chengdu, Sichuan, China
Work mode:
Onsite
Published on:
11 September 2026
What they need
该职位来源于猎聘 职责描述: 1.按照GCP法规要求及项目所需,开展研究中心调研,筛选出具备资质和足够资源的研究者; 2.按照监查计划和适用的监查规程实施监查,督促研究团队按照方案实施,确保临床试验数据的真实、完整、准确; 3.根据临床试验项目的工作计划,积极主动与研究团队保持良好沟通,保证试验中心项目按时完成; 4.负责对CRC进行项目培训,并做好项目实施的监督管理; 5.如出现偏离试验方案、SOP及相关法律法规的情况,需及时与研究团队沟通,并采取适当措施避免同类问题的重复发生。 任职要求: 1、本科及以上学历,中医、中西医结合、西医临床、中药等医药相关专业; 2、沟通能力强、获得奖学金者优先; 3、熟悉临床试验相关法规及工作流程; 4、具备良好的沟通协调能力,善于发现并解决问题。
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