临床监查员 - Chengdu
1周前
Job summary
The job involves performing and coordinating all aspects of clinical monitoring and site management. It requires conducting remote or on-site visits to assess protocol and regulatory compliance, managing required documentation, and ensuring data accuracy through SDR, SDV, and CRF review as applicable.Key responsibilities include escalating observed deficiencies, participating in investigator meetings, identifying potential investigators,
ensuring that required essential documents are complete
- Maintains regular contact with investigative sites
- Sends trial status tracking reports
工作描述
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