Lead clinical trial excellence with flexible work arrangements. ICON is seeking an experienced Senior Clinical Research Associate in Taiwan to oversee and manage clinical trial sites while enjoying a balanced hybrid work model. In this senior role, you will ensure protocol compliance, data integrity, and patient safety across multiple sites, leveraging your extensive monitoring expertise to drive successful trial execution in the Taiwanese market.
Key Responsibilities
You will be the primary point of contact for clinical trial sites, ensuring excellence in monitoring and site management.
Site Management & Monitoring:
- Conduct comprehensive site monitoring visits to ensure adherence to protocol, GCP standards, and Taiwanese regulatory requirements
- Perform source data verification and review case report forms to maintain the highest data quality standards
- Build and maintain effective relationships with site personnel and stakeholders to facilitate smooth trial operations
Quality Assurance & Mentorship:
- Provide training and guidance to site staff and junior CRAs to maintain high standards of clinical trial conduct
- Identify and resolve complex site issues, implementing corrective actions when necessary
- Collaborate with cross-functional teams to ensure timely and accurate data collection and reporting
Compliance & Risk Management:
- Ensure all site activities comply with ICH-GCP guidelines and local Taiwanese regulations
- Proactively identify and mitigate risks to patient safety and data integrity
- Maintain complete and accurate monitoring documentation
Your Profile
Essential Qualifications:
- Advanced degree in Life Sciences, Nursing, Medicine, or related field
- Extensive experience as a CRA with proven success in clinical trial monitoring
- Comprehensive knowledge of ICH-GCP guidelines and Taiwanese regulatory requirements
Required Skills & Availability:
- Proven ability to manage multiple sites and projects simultaneously
- Strong organizational, problem-solving, and stakeholder management skills
- Expertise in clinical trial software and monitoring practices
- Ability to travel approximately 60% (domestic/international) with valid driver's license
- Excellent communication and interpersonal skills
Why Join ICON?
Our success depends on our people. When you join ICON, you become part of a team dedicated to excellence in clinical development. We offer:
- Flexible Work Model: Client office-based with work-from-home flexibility
- Competitive Salary and comprehensive benefits package
- Health Insurance and retirement planning options
- Global Employee Assistance Programme and extensive well-being support
- A diverse, inclusive culture that rewards high performance
Ready to advance your clinical research career with flexible work options? We encourage you to apply even if you don't meet every single requirement. Your monitoring expertise in the Taiwanese market is highly valuable to our mission.
