Advance your career as a Clinical Research Associate with ICON plc in Quebec City. This home-based role focuses on clinical trials and data integrity while collaborating with site staff.

ICON plc is looking for a Clinical Research Associate to join its innovative team. Your responsibilities will include site qualification, monitoring, and ensuring protocol compliance throughout clinical trials. With a minimum of 9 months of onsite monitoring experience, you will help shape the future of clinical development while working independently and collaboratively.

Key Responsibilities:
• Conduct site qualification and initiation for clinical trials
• Monitor adherence to protocols and patient safety
• Collaborate with investigators and site personnel




• Review data and resolve queries for accuracy
• Prepare and review clinical study documentation

Requirements:
• Bachelor's degree in a scientific or healthcare field
• Minimum 9 months experience as a Clinical Research Associate
• In-depth knowledge of clinical trial processes
• Robust communication skills in English and French
• Willingness to travel 60% of the time

Engage in the evolution of innovative treatments as a pivotal Clinical Research Associate at ICON in Quebec.
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📌 Clinical Research Associate Remote Quebec (New Brunswick)
🏢 ICON Strategic Solutions
📍 New Brunswick