Clinical Research Associate II/ Senior Clinical Research Associate
ICON · Hong Kong
Clinical OperationsFull-timeCompany career page
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Role summary
ICON seeks a Senior Clinical Research Associate to oversee clinical trial activities in Hong Kong, ensuring protocol adherence, regulatory compliance, and data integrity across multiple sites. The role involves monitoring, site visits, team collaboration, and staff training within a global clinical research organization.
What they're looking for
- Advanced degree in life sciences, nursing, medicine, or related field
- Extensive experience as a Clinical Research Associate with deep knowledge of trial processes
- Demonstrated ability to manage multiple sites and projects concurrently
- Expertise in monitoring practices, data integrity, and clinical trial software systems
- Strong communication, interpersonal, and stakeholder management capabilities
- Valid driver's license and willingness to travel 60% (international and domestic)
What you'll be doing
- Monitor clinical trial sites for adherence to protocols, regulations, and GCP standards
- 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 and mentor site staff and other CRAs on clinical trial conduct standards
- Develop and sustain relationships with site personnel and stakeholders for trial success
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.