FSP CRA I/CRA II (Guangzhou)
Fortrea · Guangdong, China
Clinical OperationsFull timeCompany career page
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Role summary
Fortrea seeks a Clinical Research Associate to oversee site monitoring and management for clinical studies in Guangzhou. The role encompasses study initiation, data integrity verification, regulatory compliance, and vendor coordination across assigned projects.
What they're looking for
- University degree or allied health certification (e.g., nursing); equivalent experience considered
- Six months prior experience in site management, CRA, study coordination, or related clinical role
- Fluent in local language and English, written and verbal
- Basic knowledge of regulatory guidelines and clinical trial processes
- Valid driver's license; willingness to travel internationally
- Proficiency with computer systems and Microsoft Office applications
- Strong organizational, planning, and problem-solving capabilities
What you'll be doing
- Conduct routine site monitoring, pre-study visits, and study closeout activities
- Verify informed consent procedures and protocol adherence; ensure patient protection
- Review source documents and Case Report Forms for data accuracy and completeness
- Track Serious Adverse Events; prepare reports and follow-up documentation
- Manage vendor relationships, investigator budgets, and clinical trial supplies coordination
Privacy & handoff
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