Senior CRA
ICON · SC +1 more
Clinical OperationsFull-timeCompany career page
RoleLantern re-checked this role's application link recently and it was active — the employer has not confirmed it directly.
Role summary
Senior Clinical Research Associate at ICON overseeing clinical trial monitoring activities across sponsor-dedicated engagements. The role focuses on ensuring protocol adherence, regulatory compliance, and data integrity while leading site management and mentoring junior staff.
What they're looking for
- Bachelor's degree in relevant scientific or healthcare discipline
- Extensive Clinical Research Associate experience with deep knowledge of trial processes
- Demonstrated ability to manage multiple sites and projects concurrently
- Proficiency in monitoring practices, data integrity, and clinical trial software systems
- Strong communication, interpersonal, and stakeholder management capabilities
- Willingness to travel approximately 60% as required
- Legal authorization to work in assigned country
What you'll be doing
- Monitor clinical trial sites for protocol adherence, regulatory compliance, and GCP standard adherence
- Conduct site visits to evaluate performance, resolve operational issues, and provide ongoing support
- Collaborate with cross-functional teams on timely and accurate data collection and reporting
- Train and mentor site staff and junior CRAs to maintain high-quality trial conduct standards
- Build and maintain effective relationships with site personnel and stakeholders
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.