Clinical Research Associate
ICON · Beijing, China
Clinical OperationsFull-timeCompany career page
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Role summary
Clinical Research Associate role based in Beijing, responsible for conducting site visits, monitoring trial protocols, and ensuring data integrity across clinical studies. Requires a bachelor's degree in a scientific field and minimum two years of CRA experience, with strong knowledge of ICH-GCP guidelines and willingness to travel approximately 60%.
What they're looking for
- Bachelor's degree in scientific or healthcare-related field
- Minimum 2 years of clinical research associate experience
- 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 trials
- Ensure protocol compliance, data integrity, and patient safety throughout trial process
- Collaborate with investigators and site staff to facilitate study conduct
- Perform data review and resolve queries to maintain high-quality clinical data
- Prepare and review study documentation including protocols and clinical study reports
Privacy & handoff
This role links to ICON's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.