CRA II
ICON · Seoul, South Korea
The apply link worked recently (not employer-confirmed).
Role summary
Clinical Research Associate II position focused on oncology trial monitoring, based in Seoul with home-based flexibility. Responsibilities include site qualification, protocol compliance monitoring, data integrity verification, and study documentation review. Requires a bachelor's degree in a scientific field, minimum two years of CRA experience with Phase I oncology studies, 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
- Deep 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%
- Global oncology Phase I studies experience as CRA
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
- Review data and resolve queries to maintain high-quality clinical data
- Prepare and review study documentation including protocols and 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.