FSO CRA II(Guangzhou/Fuzhou/Shenzhen)

Fortrea · Guangdong, China

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Clinical OperationsFull timeCompany career page

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Role summary

Fortrea seeks a Clinical Research Associate II to manage clinical trial sites across Guangzhou, Fuzhou, or Shenzhen. The role involves site monitoring, data integrity oversight, regulatory compliance, and investigational product accountability according to ICH GCP guidelines and company procedures.

What they're looking for

University degree or allied health certification (e.g., nursing licensure)
Minimum 2 years of clinical monitoring experience
Fluent in local office language and English, written and verbal
Thorough understanding of ICH GCP guidelines and local regulatory requirements
Ability to monitor sites independently with minimal supervision
Knowledge of serious adverse event reporting and follow-up processes

What you'll be doing

Manage assigned clinical trial sites per SOPs, ICH GCP guidelines, and sponsor requirements
Conduct pre-study, initiation, routine, and closeout monitoring visits; prepare project plans
Perform source document review, verification, query generation, and data integrity oversight
Verify informed consent procedures, protocol adherence, and subject protection compliance
Track investigational product inventory, ensure regulatory document completeness, and maintain audit readiness

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What RoleLantern checked

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Date posted7 days ago

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