Clinical Research Associate

Senior Clinical Research Associate position at ICON in Quebec City focused on monitoring cardiovascular and respiratory clinical trials. The role requires overseeing site activities, ensuring protocol compliance, and managing relationships with clinical trial sites while working independently and mentoring other CRAs.

Responsibilities

• 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 with cross-functional teams to ensure accurate and timely data collection and reporting
• Provide training and guidance to site staff and other CRAs to maintain high conduct standards
• Build and maintain relationships with site personnel and stakeholders to facilitate trial operations

Requirements

• Bachelor's degree in relevant scientific or healthcare field
• Extensive experience as Clinical Research Associate with strong understanding of trial processes
• Demonstrated ability to manage multiple sites and projects simultaneously
• Expertise in monitoring practices, data integrity, and clinical trial software tools
• Strong communication, interpersonal, and stakeholder management skills
• Willingness to travel approximately 60% as required
• Legal right to work in Canada