Advance your career as a Senior Clinical Research Associate at ICON Strategic Solutions, where you’ll support complex clinical studies in a cooperative team workplace.

At ICON, the largest FSP organization, your role involves independent monitoring of investigational sites through phases II-IV. You will prepare documentation for regulatory submissions and ensure adherence to ICH-GCP principles. Your skills will help enhance training for fellow CRAs while contributing to global health advancements.

Key Responsibilities:
• Independent setup and monitoring of clinical trials
• Complete submissions for ethics and regulatory approval
• Manage study cost efficiency throughout the process
• Review documentation for feasibility studies
• Mentor and train junior Clinical Research Associates

Requirements:
• 18+ months of phase I-III monitoring experience
• Prior involvement in medium-sized studies
• Familiarity with ICH-GCP guidelines
• Solid ability to meet critical deadlines
• 60% travel availability with a valid driver’s license

Join ICON to make a global impact on healthcare innovation and patient outcomes.
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📌 Senior Clinical Research Associate Role Ontario (Canada)
🏢 ICON Strategic Solutions
📍 Canada