Senior Clinical Research Associate
ICON · Montreal, Canada +1 more
Clinical OperationsFull-timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
Senior Clinical Research Associate role at ICON in Quebec City focused on cardiovascular and respiratory clinical trial monitoring. Oversee site compliance with protocols, regulatory requirements, and GCP standards while managing multiple projects and mentoring clinical research staff.
What they're looking for
- Bachelor's degree in relevant scientific or healthcare discipline
- Extensive clinical research associate experience with deep understanding of trial processes
- Proven ability to manage multiple sites and projects simultaneously
- Expertise in monitoring practices, data integrity, and clinical trial software systems
- Strong communication and stakeholder management skills with compliance influence ability
- Willingness to travel approximately 60% of the time
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 issues, and provide operational support
- Collaborate across teams to ensure timely and accurate data collection and reporting
- Provide training and guidance to site staff and other CRAs on clinical trial standards
- Build and maintain effective relationships with site personnel and key 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.