代po 【职缺名称】CRA 【徵才单位】Parexel 百瑞精鼎 【工作地址】台北市信义区基隆路一段200号22楼 【工作内容】 1. Conduct qualification visits (QV), site initiation visits (SIV), monitoring visits (MV) and termination visits (TV) at assigned clinical sites and genera te visit/contact reports. 2. Oversee integrity of the study and utilize problem-solving skills to promot e rapport with the site and staff. 3. Review the performance of the trial at designated sites, ensure the rights and well-being of human subjects are safeguarded and are in accordance with pr otocol. 4. Develop patient recruitment strategies in conjunction with the clinical sit e to meet enrollment timelines, while also ensuring compliance with the approv ed standard operating procedures (SOPs), protocol/amendment(s), GCP, and the a pplicable regulatory requirement(s). 5. Evaluate the quality and integrity of the reported data, site efficacy and drug accountability. 6. Monitor the completeness and quality of Regulatory Documentation and perfor m site document verification. 【徵才条件】 1. 1年以上临床试验监测经验 2. 英语： 听说读写 中等以上 3. IRB 送审经验 佳 4. phase II/III 经验 佳 【薪资待遇】面议 【联络方式】有意者，请站内信 ※ 编辑: hippo11915 (111.71.40.163 台湾), 12/22/2021 23:55:47