Clinical Research Associate II, China
About this role
About the Role ICON is seeking a Clinical Research Associate II in China to design and analyse clinical trials, interpret complex medical data, and contribute to advancing innovative treatments. The role focuses on monitoring activities and ensuring trial integrity, patient safety, and protocol compliance in collaboration with investigators and site staff. 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
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