Elevate your clinical research career as a Senior Clinical Research Associate at ICON Plc in the Greater Toronto Area. Focus on monitoring respiratory and cardiovascular studies while working in a supportive, global team.

As a Senior Clinical Research Associate at ICON Solutions, you will be key to managing clinical trial activities and ensuring compliance with study protocols and regulatory standards. This position requires a deep understanding of clinical trial monitoring, strong organizational skills, and the ability to work independently while mentoring others. You’ll also enjoy a collaborative culture that fosters skilled growth and the development of vital patient treatments.

Key Responsibilities:
• Monitor trial sites for protocol adherence and GCP standards
• Conduct site visits to resolve issues and support operations




• Collaborate with teams for accurate data collection
• Train site staff to uphold high clinical standards
• Build relationships with stakeholders to facilitate trials

Requirements:
• Bachelor’s degree in a relevant scientific field
• Extensive CRA experience and understanding of trial processes
• Proven multitasking abilities with organization skills
• Expertise in monitoring and site management
• Excellent communication and interpersonal skills

Drive clinical research excellence by applying your expertise in monitoring and support at ICON Plc in the GTA.
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📌 Senior Clinical Research Associate GTA (Quebec City)
🏢 ICON Clinical Research
📍 Quebec City