Senior CRA

ICON · Chengdu, China

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Clinical OperationsFull-timeCompany career page

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Role summary

Senior Clinical Research Associate position with ICON based in Chengdu, China. The role involves designing and analyzing clinical trials, monitoring study sites, ensuring protocol compliance, and maintaining data integrity throughout the clinical trial process.

What they're looking for

Bachelor's degree in scientific or healthcare-related field
Minimum 2 years of experience as a Clinical Research Associate
In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines
Strong organizational and communication skills with attention to detail
Ability to work independently and collaboratively in fast-paced environment
Willingness to travel approximately 60% as required
Legal right to work in China

What you'll be doing

Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials
Ensure protocol compliance, data integrity, and patient safety throughout 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 preparation and review of study documentation including protocols and reports

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Date posted5 days ago

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