Clinical Research Associate II
ICON · Beijing, China +6 more
Clinical OperationsFull-timeCompany career page
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Role summary
Clinical Research Associate II role focused on monitoring clinical trials across multiple Chinese sites. Responsibilities include site qualification, protocol compliance, data integrity oversight, and documentation preparation. Requires a bachelor's degree in a science or healthcare field, minimum two years of CRA experience, ICH-GCP knowledge, and willingness to travel approximately 60%.
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, 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%
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 for clinical data quality
- Contribute to preparation and review of study documentation
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.