FSP CRA II (Zhengzhou)

Fortrea · Shanghai, China

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Clinical OperationsFull timeCompany career page

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Role summary

Fortrea seeks a Clinical Research Associate II based in Zhengzhou to manage clinical trial sites, conduct monitoring visits, verify data integrity, and ensure regulatory compliance according to ICH GCP guidelines and company procedures.

What they're looking for

University degree or allied health certification (nursing or equivalent experience)
Minimum 2 years clinical monitoring experience
Fluent in local 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 monitoring procedures

What you'll be doing

Manage assigned clinical trial sites and conduct pre-study, initiation, routine, and closeout monitoring visits
Perform source document verification, identify data discrepancies, and generate queries for resolution
Verify informed consent procedures, protocol adherence, and subject protection compliance
Track investigational product inventory, ensure secure storage, and maintain regulatory documentation
Travel to sites as required and prepare accurate trip reports and monitoring deliverables

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Date posted4 days ago

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