FSP CRA(Level II)
Thermo Fisher Scientific · Sichuan, China
RoleLantern re-checked this role's application link recently and it was active — the employer has not confirmed it directly.
Role summary
Thermo Fisher Scientific seeks a Level II Clinical Research Associate to monitor investigational sites, ensure protocol compliance, and manage clinical trial documentation. The role involves remote and on-site visits across multiple trial environments, with responsibility for data accuracy, regulatory adherence, and collaborative site management.
What they're looking for
- Bachelor's degree in life sciences or registered nursing certification
- Approximately one year of clinical research monitoring experience or equivalent
- Proficiency in ICH-GCP guidelines and applicable regulations
- Strong critical thinking, root cause analysis, and problem-solving abilities
- Demonstrated medical/therapeutic area knowledge and terminology expertise
- Excellent written and oral communication skills
- Valid driver's license where applicable
What you'll be doing
- Conduct risk-based monitoring of investigator sites using root cause analysis to identify process failures and corrective actions
- Perform source document review, verification, and CRF assessment via on-site and remote monitoring activities
- Initiate clinical trial sites, facilitate investigator meetings, and manage trial closeout procedures
- Maintain essential document completion and compliance per ICH-GCP standards through on-site file reviews
- Provide trial status updates and reports to clinical management, facilitating communication between sites and sponsor companies
Privacy & handoff
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