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Clinical Research Associate (EG-090 or 100, Permanent)
On-site · Seoul, Seoul, South Korea
Job Summary
Clinical Research Associate responsible for site qualification, initiation, routine monitoring and close-out visits across trial phases, ensuring adherence to protocol, ICH GCP and local regulations. Maintains data integrity by verifying data in electronic and paper records, supports audits/inspections, fosters relationships with clinical sites and vendors, monitors enrollment/retention, prepares timely monitoring and administrative reports, assesses site resources, and uses centralized/remotebased monitoring approaches. May lead CRA activities and provide mentorship; requires proficiency with CTMS/eDC/eTMF/RBM tools and ability to manage multiple protocols and travel as needed. On-site roles described as site-essential or hybrid/remote-by-design depending on occupancy structure.
Required Qualifications
- Bachelor’s degree in life sciences or equivalent
- Ability to work independently with a high degree of autonomy
- Experience in clinical research monitoring activity (1-5+ years depending on level)
- Proficiency with clinical systems (CTMS, eTMF, eDC, RBM tools)
- Strong communication skills in English and local language
- Driver’s license may be required locally
- Ability to travel across multiple protocols/therapeutic areas as needed
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