Join Pfizer as a Senior Clinical Research Associate I to oversee site management and monitoring in clinical trials. Ensure patient safety and compliance while enhancing study quality and investigator relations.

As a Senior Clinical Research Associate I, you will manage and monitor assigned clinical trial sites, guaranteeing compliance with Good Clinical Practices and regulations. Your role involves facilitating effective communication between investigators and the study team, supporting patient recruitment, and conducting in office monitoring. By maintaining high standards, you will reinforce both quality and safety throughout the trial process while enhancing the company's image.

Key Responsibilities:
• Manage site operations and ensure quality delivery of trials




• Conduct on-site and remote monitoring for compliance
• Train and support site staff in protocol adherence
• Resolve protocol-related issues efficiently
• Submit required reports and documentation on time

Requirements:
• Bachelor's in Life Sciences or related field
• Minimum 3 years of monitoring experience in clinical research
• Experience in Oncology preferred
• Proficient in English
• Willingness to travel 60-80%

Bring your expertise in clinical trials and commitment to quality to Pfizer as a Senior Clinical Research Associate I.
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📌 Clinical Research Associate Senior at Pfizer (Manitoba)
🏢 Pfizer
📍 Manitoba