(Senior or Lead) Clinical Research Associate
ICON · Taipei, Taiwan
Clinical OperationsFull-timeCompany career page
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Role summary
ICON seeks a Clinical Research Associate II to conduct site visits, ensure protocol compliance, and manage data quality for clinical trials. The role involves monitoring study conduct, collaborating with site staff, and preparing trial documentation across multiple therapeutic areas.
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 travel 60% of the time (international and domestic); valid driver's license required
- Oncology experience preferred
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 effective 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.