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Clinical Research Associate

ICON
onsite
Beijing, China

About this role

About the Role ICON is seeking a Clinical Research Associate in Beijing to monitor and support clinical trials, ensure protocol compliance and data integrity, and collaborate with investigators to advance innovative treatments. This role involves independent work and cross-functional collaboration to keep trials on track. What You'll Do

  • Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials
  • Ensure protocol compliance, data integrity, and patient safety throughout the trial process
  • Collaborate with investigators and site staff to facilitate smooth study conduct
  • Perform data review and resolution of queries to maintain high-quality clinical data
  • Contribute to the preparation and review of study documentation, including protocols and clinical study reports What We're Looking For
  • Bachelor's degree in a scientific or healthcare-related field

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