CRA1/2/Sr（Drug)-KunTuo
IQVIA · Beijing, China +1 more
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Role summary
Clinical research associate responsible for site selection, initiation, monitoring, and closeout activities across multiple studies and therapeutic areas in accordance with protocols, contracts, SOPs, and GCP requirements. Duties include training research sites, managing regulatory submissions and recruitment tracking, assessing data quality, maintaining documentation, and overseeing study finances at assigned sites.
What they're looking for
- Knowledge of GCP guidelines and clinical trial protocols
- Experience monitoring multiple clinical trial sites simultaneously
- Ability to assess data quality and regulatory compliance
- Strong communication skills for site coordination and training
- Documentation and financial management capabilities for research sites
What you'll be doing
- Conduct site selection, initiation, monitoring, and closeout visits per protocol and SOP requirements
- Manage progress across assigned sites by tracking enrollment, CRF submissions, and data queries
- Provide protocol and study-related training to research centers with regular communication
- Evaluate quality and completeness of site work; escalate compliance issues to PM or manager
- Create and maintain monitoring documentation, visit reports, and action plans; manage site finances
Privacy & handoff
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