CRA II
ICON · Seoul, South Korea
Clinical OperationsFull-timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
Clinical Research Associate II position focused on designing and analyzing clinical trials while monitoring study sites. The role involves ensuring protocol compliance, data integrity, and patient safety across multiple trial activities in a collaborative clinical research environment.
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 settings
- Willingness to travel approximately 60% as required
- Legal right to work in South Korea
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 processes
- Collaborate with investigators and site staff to facilitate smooth 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.