💊 Advance Patient Access as Clinical Trial Administrator - South Korea
Join ICON plc in South Korea as a Clinical Trial Administrator and play a crucial role in managing therapeutic access programs that provide hope and treatment options for patients with serious medical conditions. This office-based position offers the opportunity to ensure compliant access to investigational medicines while supporting clinical research excellence.
🎯 Your Impact: Key Responsibilities
Therapeutic Access Program Management
- Manage the provision of access to investigational or unapproved products outside clinical trials
- Facilitate patient access to medications for serious or life-threatening conditions when no other options exist
- Oversee MAP (Managed Access Program) status system management and documentation
- Ensure compliant pre-approval drug supply and access for eligible patients
Clinical Trial Documentation & Compliance
- Maintain essential documents in accordance with regulatory requirements
- Manage clinical drug supplies and inventory tracking
- Conduct safety-related checks and support SAE reconciliation processes
- Handle cost management and budget tracking for access programs
Stakeholder Coordination & Communication
- Maintain proactive communication with principal investigators and medical professionals
- Coordinate with cross-functional teams to ensure program success
- Support Investigator-Initiated Trial (IIT) activities and site coordination
- Serve as a reliable point of contact for program-related inquiries
Quality Assurance & Process Excellence
- Ensure all activities comply with regulatory standards and company SOPs
- Maintain accurate records and documentation for audit readiness
- Support continuous improvement of access program processes
- Demonstrate flexibility and ownership in managing program responsibilities
⭐ Your Profile: Qualifications & Experience
Essential Requirements
- Bachelor's degree in scientific or healthcare-related field
- Previous experience as CTA or CRA required
- Knowledge of clinical trial processes, regulations, and guidelines
- Experience with site coordination (SC) or Investigator-Initiated Trials (IIT)
Professional Competencies
- Excellent organizational skills with strong attention to detail
- Effective communication skills in Korean and English
- Ability to work collaboratively in fast-paced environments
- Flexibility and ownership mindset for program management
Preferred Qualifications
- Experience in therapeutic access programs or managed access systems
- Background in clinical supply management and documentation
- Understanding of safety reporting and SAE reconciliation processes
- Site coordination experience in clinical research settings
💫 Why Join ICON in South Korea?
Meaningful Patient Impact
- Provide access to potentially life-saving treatments for patients with unmet medical needs
- Work at the forefront of therapeutic access and clinical research
- Support Korean patients in accessing innovative medical treatments
- Contribute to advancing healthcare options in South Korea
Professional Development
- Clear career pathway in clinical research administration
- Exposure to global access programs and regulatory requirements
- Opportunities for advancement within ICON's growing Korean operations
- Comprehensive training in therapeutic access program management
Office-Based Advantages
- Stable office environment with professional workspace
- Direct collaboration with local and international team members
- Structured work schedule with work-life balance
- Modern office facilities and technology support
Competitive Korea Benefits
- Attractive salary package with performance incentives
- Comprehensive health insurance for you and your family
- Global Employee Assistance Programme with 24/7 support
- Generous annual leave and public holiday observance
Additional Global Benefits
- Retirement planning and pension benefits
- Life assurance coverage
- Professional development opportunities
- Health and wellness programs
- Team building and cultural events
✨ Ready to Facilitate Critical Patient Access?
If you're an experienced clinical research professional with CTA or CRA background and passion for helping patients access vital treatments, we encourage you to apply. This role offers the unique opportunity to manage therapeutic access programs that bring hope to patients while advancing clinical research in South Korea.
Apply Now & Join Our Korea Clinical Operations Team!
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ICON is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status.
We welcome applications from all qualified clinical professionals in South Korea - your experience in clinical research administration might be exactly what we need at ICON!
