Clinical Research Associate Job at ICON
Looking for a Clinical Research Associate Job with a leading global CRO? ICON is hiring a Clinical Research Associate I (CRA I) to support oncology clinical trials in a remote, home-based role in South Korea. Professionals searching for ICON Careers and exciting Clinical Research Jobs can join a world-renowned organisation, contribute to innovative clinical development, and work alongside global research teams dedicated to improving patient outcomes.
About the Company:
ICON plc is a global healthcare intelligence and clinical research organization that partners with pharmaceutical, biotechnology, and medical device companies to accelerate clinical development. With a strong commitment to innovation, diversity, and scientific excellence, ICON delivers high-quality clinical research solutions across the world. Through ICON Strategic Solutions, employees gain access to exciting career opportunities, cutting-edge clinical trials, and a collaborative environment that supports continuous professional growth.
Job Details:
- Job Title: Clinical Research Associate I (CRA I)
- Job Reference: JR154059
- Department: Clinical Monitoring
- Location: Seoul, South Korea
- Work Mode: Remote (Home-Based)
- Therapeutic Area: Oncology
- Employment Type: Full-Time
Job Description:
ICON Strategic Solutions (FSP) is seeking a Clinical Research Associate I (CRA I) to join its Clinical Monitoring team. This Clinical Research Associate Job is a home-based opportunity in South Korea, focusing on oncology clinical trials. The selected candidate will coordinate clinical trial activities, monitor study progress, ensure compliance with ICH-GCP guidelines, and maintain strong relationships with investigators and study sites. Candidates exploring ICON Careers and Clinical Research Jobs will benefit from working in a globally recognized CRO known for innovation and career development.
Key Responsibilities:
- Coordinate clinical trial start-up and monitoring activities.
- Monitor study progress and maintain study documentation.
- Prepare accurate study status reports.
- Resolve sponsor-generated queries efficiently.
- Support feasibility studies and study documentation.
- Build strong relationships with investigators and site staff.
- Ensure compliance with ICH-GCP guidelines and regulatory requirements.
- Promote patient safety and data quality throughout clinical trials.
Educational Requirements for this Clinical Research Associate Job:
Essential Qualification
- Bachelor’s degree or equivalent in Medicine, or a related field.
Experience & Requirements
- Knowledge of ICH-GCP guidelines.
- Ability to review and evaluate medical data.
- Excellent written and verbal communication skills in English.
- Strong interpersonal and organizational skills.
- Willingness to travel approximately 60% as required.
Skills Required for this Clinical Research Associate Job:
- Clinical Trial Monitoring
- Clinical Research
- ICH-GCP Compliance
- Oncology Research
- Clinical Documentation
- Site Management
- Medical Data Review
- Regulatory Compliance
- Clinical Operations
- Communication Skills
- Stakeholder Management
- Problem Solving
- Time Management
- Team Collaboration
- Patient Safety
