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FSO CRA II(Changsha)

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 in Changsha to manage clinical trial sites, conduct monitoring visits, ensure regulatory compliance, and maintain data integrity 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 clinical monitoring experience
  • Thorough knowledge of ICH GCP guidelines and local regulatory requirements
  • Fluent in local office language and English, written and verbal
  • Ability to monitor sites independently with minimal supervision
  • Understanding of serious adverse event reporting and clinical trial processes

What you'll be doing

  • Manage clinical study sites per SOPs, ICH GCP, and sponsor requirements
  • Conduct site initiation, routine, and closeout monitoring visits
  • Verify informed consent, protocol adherence, and subject protection measures
  • Review source documents, identify discrepancies, and generate data queries
  • Track investigational product inventory and ensure regulatory document completeness

Privacy & handoff

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What RoleLantern checked

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RoleLantern checked active
RoleLantern checkedNeeds clarity
Date posted7 days ago
Last source checkToday
Salary listedNeeds clarity
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