Clinical Research Associate I
Remote · Seoul, Seoul, South Korea
Job Summary
Monitor oncology clinical trials and manage activities to ensure high-quality outcomes across programmes. Responsibilities include coordinating setup and monitoring of studies, producing accurate study status reports and documentation, efficiently handling sponsor queries, and participating in feasibility studies for new proposals. Build and maintain strong relationships with key stakeholders, clinical investigators, and site staff, while ensuring patient safety and adherence to ICON procedures, protocols, and regulatory requirements. Travel approximately 60% and operate in a home-based/remote capacity.
Required Qualifications
- University degree in medicine, science, or equivalent
- Knowledge of ICH-GCP guidelines
- Excellent written and verbal communication in English
- Willingness to travel as required (approximately 60%)
- Oncology studies experience is a must
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