Elevate your career as a Clinical Trial Associate with ICON in Mississauga, Ontario. This hybrid role focuses on oncology research, trial coordination, and regulatory compliance.
In this dynamic position, you will support clinical trial design and execution while ensuring regulations are met. Collaborate closely with teams and stakeholders to deliver quality research outcomes. Your contributions will assist in advancing innovative therapies and manage complex medical data to drive clinical excellence.
Key Responsibilities:
• Coordinate and administer clinical trials to ensure compliance
• Organize clinical trial documentation and essential study files
• Prepare study-related materials, including consent forms




• Facilitate communication within cross-functional teams
• Track and report clinical trial metrics and milestones
Requirements:
• Bachelor’s degree in a scientific or healthcare field
• Experience or strong interest in clinical research
• Knowledge of clinical trial regulations and guidelines
• Strong organizational and communication skills
• Experience in oncology studies required
Join ICON to contribute to pioneering clinical research and advance your qualified journey.
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📌 Clinical Trial Associate at ICON (Mississauga)
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📍 Mississauga