Clinical Research Associate
ICON · Seoul, South Korea
Clinical OperationsFull-timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
This Clinical Research Associate position involves coordinating clinical trial setup and monitoring activities, managing sponsor queries, and maintaining study documentation. The role requires at least two years of on-site monitoring experience, a science degree, knowledge of ICH-GCP guidelines, and approximately 60% travel. The position is home-based in Seoul, South Korea.
What they're looking for
- University degree in medicine, science, or equivalent field
- Knowledge of ICH-GCP guidelines and ability to review medical data
- Excellent written and verbal English communication skills
- At least 2 years of on-site monitoring experience in clinical trials
- Willingness to travel approximately 60% of the time
- Oncology experience preferred
What you'll be doing
- Coordinate study setup and monitoring activities while maintaining accurate documentation
- Process sponsor-generated queries and manage study cost efficiency
- Prepare and review study documentation for new proposals as needed
- Build collaborative relationships with investigators, sponsors, and site staff
- Ensure patient safety and regulatory compliance with protocols and procedures
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.