FSP CRA I (Nanning/Fuzhou/Xiamen)
Fortrea · Guangdong, China
RoleLantern re-checked this role's application link recently and it was active — the employer has not confirmed it directly.
Role summary
Fortrea seeks a Clinical Research Associate I to oversee site monitoring and management for clinical studies across Nanning, Fuzhou, or Xiamen. The role involves conducting routine site visits, ensuring protocol compliance, maintaining study documentation, and managing vendor relationships while adhering to regulatory guidelines and company procedures.
What they're looking for
- University degree or allied health certification (e.g., nursing licensure); equivalent experience acceptable
- Minimum six months experience in related clinical or site management role
- Basic knowledge of regulatory guidelines and clinical trial processes
- Fluent in local office language and English, both written and verbal
- Valid driver's license and ability to travel frequently
- Strong organizational, planning, and problem-solving skills
- Proficiency with standard computer applications and data management systems
What you'll be doing
- Conduct routine site monitoring visits, pre-study initiation, and protocol closeout activities
- Verify informed consent procedures and protocol adherence; review source documents for data integrity
- Generate and resolve Case Report Form queries using data management systems
- Track and coordinate Serious Adverse Event reporting, narratives, and follow-up documentation
- Manage investigator site budgets, vendor relationships, and study supply coordination
Privacy & handoff
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