职责
The CRA/CRC is responsible for the monitoring or auditing of all activities subject to the, “ICH良好的临床实践: 合并指南,” (GCPS), 由Watermark管理的支持客户程序确保项目数据和摘要声明具有已知和记录的质量.
要求
Will be expected to travel extensively to study sites in the US to monitor our clinical and outcome studies.
Successful applicant must have previous experience monitoring clinical trials.
全球监管要求和/或药品开发实践的基础知识.
对法规机构的方法和观点的了解/理解.
基本技能和能力
良好的书面和口头沟通技巧, demonstrated ability to function effectively with all levels of management
强大的谈判和建立关系技巧
Good understanding of medical / corporate governance principles
Detailed oriented and organized
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