精鼎医药研究开发（上海）有限公司招聘临床监察员CRA

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精鼎医药研究开发（上海）有限公司 —— 临床监察员/CRA

岗位要求：

The responsibility of a Clinical Research Associate (CRA) is to perform the clinical monitoring aspect

of designated projects in accordance with applicable SOPs and regulations. Responsibilities include

performing clinical on-site monitoring activities (drive patient recruitment, source data verification,

drug accountability, data collection), collecting regulatory documentation (when required), performing

qualification, initiation, monitoring and termination of investigational sites in accordance with ICH

GCP guidelines.

每一件事都要用多方面的角度来看它。 -@YingJieSheng.COM-

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