Clinical Research Associate
ICON · Canada
The apply link worked recently (not employer-confirmed).
Role summary
A Clinical Research Associate is needed in Canada to oversee clinical trial activities across multiple sites, ensuring compliance with protocols, regulatory standards, and Good Clinical Practice requirements. The role involves site monitoring, staff training, data integrity verification, and stakeholder collaboration. An advanced degree in life sciences or related field and extensive CRA experience with strong organizational and regulatory knowledge are required.
What they're looking for
- Advanced degree in life sciences, nursing, or medicine
- Extensive clinical research associate experience with trial process knowledge
- Ability to manage multiple sites and projects with strong organizational skills
- Expertise in monitoring practices, data integrity, and site management
- Proficiency in clinical trial software and relevant tools
- Strong communication and stakeholder management abilities
What you'll be doing
- Monitor clinical trial sites for protocol adherence and GCP standard compliance
- Conduct site visits to assess performance, resolve issues, and provide operational support
- Collaborate with cross-functional teams on accurate data collection and reporting
- Train site staff and other associates on clinical trial conduct standards
- Build and maintain relationships with site personnel to support 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.