🏠 Lead Oncology Clinical Trials as Senior CRA - South Korea (Home Based)
Join ICON plc as a Senior Clinical Research Associate in South Korea and bring your oncology expertise to global cancer research. This home-based role offers the flexibility to work from anywhere in South Korea while leading critical oncology clinical trials that advance cancer treatment and patient care worldwide.
🎯 Your Impact: Key Responsibilities
Oncology Trial Leadership & Oversight
- Monitor clinical trial sites across South Korea to ensure strict adherence to oncology study protocols and GCP standards
- Conduct comprehensive site visits to assess performance and resolve complex issues in global oncology studies
- Serve as oncology subject matter expert for multiple sites and projects throughout South Korea
- Provide strategic oversight to maintain the highest standards in oncology clinical trial conduct
Site Management & Relationship Building
- Build and maintain effective relationships with oncology investigators, site staff, and key stakeholders
- Provide expert training and guidance to site staff and junior CRAs in oncology-specific protocols
- Facilitate smooth trial operations through proactive communication and problem-solving in Korean and English
- Serve as primary point of contact for oncology site-related matters and escalations
Data Integrity & Quality Assurance
- Ensure timely and accurate data collection and reporting across all assigned oncology sites
- Collaborate with cross-functional teams to maintain data integrity throughout oncology study lifecycle
- Implement quality control measures specific to oncology trial requirements
- Utilize clinical trial software and tools to optimize monitoring efficiency in cancer research
Compliance & Risk Management in Oncology
- Drive compliance within South Korea's regulatory environment for oncology clinical trials
- Identify and mitigate potential risks to oncology trial timelines and data quality
- Ensure patient safety remains paramount in oncology studies with complex treatment regimens
- Maintain audit-ready documentation for global oncology regulatory submissions
⭐ Your Profile: Qualifications & Experience
Essential Requirements
- Advanced degree in life sciences, nursing, medicine, or related field
- Extensive experience as a Clinical Research Associate with proven track record in global oncology studies
- Strong understanding of oncology clinical trial processes and regulatory requirements
- Must have direct experience with global oncology clinical trials
Oncology-Specific Expertise
- Comprehensive knowledge of oncology protocols and cancer treatment methodologies
- Experience with oncology-specific endpoints and response criteria
- Understanding of oncology patient management and supportive care requirements
- Familiarity with oncology imaging requirements and tumor assessment protocols
Technical Competencies
- Proficiency in clinical trial software and monitoring tools
- Expertise in monitoring practices and data integrity in oncology trials
- Experience managing multiple oncology sites and projects simultaneously
- Strong organizational and problem-solving capabilities for complex oncology studies
Professional Attributes
- Excellent communication and interpersonal skills in Korean and English
- Ability to influence and drive compliance in complex oncology research environments
- Strong stakeholder management and relationship-building skills
- Self-motivated with ability to work independently in home-based setting
Operational Requirements
- Ability to travel approximately 60% domestically across South Korea
- Valid driver's license for site visit requirements
- Home-based with reliable internet and dedicated workspace
- Flexibility to accommodate global team collaboration across time zones
💫 Why Join ICON in South Korea?
Professional Impact
- Lead global oncology clinical trials that advance cancer treatment worldwide
- Contribute to cutting-edge cancer research from South Korea's growing clinical landscape
- Work with innovative oncology therapies and treatment approaches
- Play a key role in ICON's expanding oncology portfolio in Asia
Home-Based Advantages
- Work from anywhere in South Korea with flexible remote arrangement
- Balance travel requirements with comfortable home office environment
- Avoid daily commute while maintaining professional collaboration
- Modern technology infrastructure for seamless virtual teamwork
Career Advancement
- Clear pathway to Clinical Team Lead and Oncology Project Management roles
- Exposure to diverse oncology indications and novel therapeutic approaches
- Opportunities for professional development in oncology specialization
- Global networking within ICON's worldwide oncology community
Competitive Korea Benefits
- Attractive salary package with performance incentives and travel allowances
- Comprehensive health insurance for you and your family
- Global Employee Assistance Programme with 24/7 support
- Generous annual leave with Korean public holidays
Additional Korea Benefits
- Retirement planning through Korean pension benefits
- Life assurance coverage
- Professional development allowance
- Health and wellness programs
- Support for home office setup and equipment
✨ Ready to Lead Oncology Clinical Research in South Korea?
If you're an experienced CRA with extensive oncology trial experience and passion for advancing cancer treatment, we encourage you to apply. This home-based role offers the perfect opportunity to leverage your oncology expertise while enjoying the flexibility of working from anywhere in South Korea and contributing to global cancer research.
Apply Now & Lead Our Oncology Clinical Trials in Korea!
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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 oncology clinical research professionals across South Korea - your global oncology expertise might be exactly what we need at ICON!
