Elevate your career as a Clinical Research Associate I with Pfizer, focusing on clinical trial management and site monitoring in oncology. This full-time role ensures patient safety and adherence to industry standards.

As a Senior Clinical Research Associate I, you will oversee assigned clinical trial sites, ensuring compliance with Positive Clinical Practices and applicable regulations. You will engage with site personnel, manage relationships, and facilitate effective data dissemination while addressing protocol-related issues. Your contributions are vital for maintaining high standards of patient safety and study quality throughout the trial phases.

Key Responsibilities:
• Manage operational aspects of clinical trials at investigator sites
• Serve as the primary contact for site-related inquiries




• Conduct onsite and remote monitoring of trial activities
• Ensure timely submission of reports and documentation
• Collaborate with site staff on recruitment and protocol adherence

Requirements:
• Bachelor’s degree in life sciences or equivalent
• Minimum 3 years of clinical research site monitoring experience
• Preferred experience in oncology or vaccine trials
• Fluent in English and local language
• Strong understanding of GCP and regulatory standards

Leverage your expertise to enhance clinical trial outcomes and impact patient safety with Pfizer.
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📌 Clinical Research Associate I at Pfizer (Ontario)
🏢 Pfizer
📍 Ontario