Clinical Research Associate II
ICON · Guangzhou, China
Clinical OperationsFull-timeCompany career page
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Role summary
Clinical Research Associate II role at ICON's Shenzhen office involving clinical trial monitoring, site management, and data quality assurance. The position requires 2+ years of CRA experience and a scientific background, with approximately 60% travel.
What they're looking for
- Bachelor's degree in scientific or healthcare-related field
- Minimum 2 years experience as 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
- Ensure protocol compliance, data integrity, and patient safety throughout trials
- Collaborate with investigators and site staff on study conduct
- Perform data review and query resolution to maintain clinical data quality
- Contribute to preparation and review of study documentation and reports
Privacy & handoff
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