Advance your career with Pfizer as a Senior Clinical Research Associate I, specializing in oncology site management and monitoring processes. This full time role is essential for maintaining clinical trial integrity and patient safety.

As a Senior Clinical Research Associate I, you will be instrumental in overseeing clinical trials across assigned sites, ensuring adherence to regulatory and GCP standards. You will manage interactions with site investigators, respond to protocol-related queries, and promote best practices for trial execution. Your role directly supports the delivery of high-quality clinical outcomes.

Key Responsibilities:
• Ensure trial compliance through proactive site management
• Act as the main point of contact for investigator sites




• Perform monitoring visits and address issues promptly
• Submit necessary documentation and reports within deadlines
• Assist in patient recruitment and site training initiatives

Requirements:
• Bachelor’s degree in life sciences or equivalent
• Minimum 3 years of clinical monitoring experience
• Preferred experience in oncology or related therapeutic areas
• Fluent in English and native language
• Comprehensive knowledge of clinical trial regulations

Contribute to advancing Pfizer's impactful clinical research while ensuring the safety and well-being of trial participants.
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📌 Senior Clinical Research Associate in Oncology (Ontario)
🏢 Pfizer
📍 Ontario