Clinical Research Associate
ICON · Burlington, Canada +1 more
Clinical OperationsFull-timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
Clinical Research Associate II position at ICON overseeing clinical trial monitoring for respiratory and cardiovascular studies in the Greater Toronto Area. The role involves site management, protocol compliance, and leading technical monitoring activities while supporting cross-functional teams and providing guidance to site staff.
What they're looking for
- Bachelor's degree in scientific discipline or healthcare-related field
- Extensive experience as Clinical Research Associate with strong clinical trial process knowledge
- Proven ability to manage multiple sites and projects simultaneously
- Expertise in monitoring practices, data integrity, and clinical trial software
- Strong communication and stakeholder management skills with ability to drive compliance
- Willingness to travel approximately 60% as required
What you'll be doing
- Monitor clinical trial sites for adherence to protocols, regulatory requirements, and GCP standards
- Conduct site visits to assess performance, resolve operational issues, and provide support
- Collaborate with cross-functional teams on accurate data collection and timely reporting
- Provide training and guidance to site staff and other CRAs on 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.