(Senior) Clinical Research Associate
ICON · Taipei, Taiwan
Clinical OperationsFull-timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
Senior Clinical Research Associate position overseeing clinical trial monitoring and site management in a sponsor-dedicated model. The role involves ensuring protocol adherence, regulatory compliance, and mentoring junior staff while managing multiple sites across trial execution.
What they're looking for
- Bachelor's degree in scientific or healthcare-related field
- Extensive clinical research associate experience with deep understanding of trial processes
- Proven ability to manage multiple sites and projects with strong organizational skills
- Expertise in monitoring practices, data integrity, and clinical trial software
- Excellent communication and stakeholder management abilities
- Willingness to travel approximately 60% as required
- Legal right to work in Taiwan
What you'll be doing
- Monitor clinical trial sites for protocol adherence, regulatory compliance, and GCP standard maintenance
- Conduct site visits to assess performance, troubleshoot issues, and provide operational support
- Collaborate with cross-functional teams on timely and accurate data collection and reporting
- Train site staff and junior CRAs to maintain high standards of trial conduct
- Build and sustain relationships with site personnel and stakeholders for smooth trial operations
Privacy & handoff
This role links to ICON's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.