Become a Senior Clinical Research Associate I at Pfizer, where you'll manage and monitor clinical trial sites ensuring compliance and high-quality study execution. Your contributions will directly impact patient safety.

This position focuses on overseeing clinical research trials at designated sites, ensuring adherence to laws and Valuable Clinical Practices. You will play a key role in tracking site progress, enhancing communication between investigators, and ensuring that all study requirements are met. Your proactive engagement will help maintain patient safety and investigator satisfaction throughout the trials.

Key Responsibilities:
• Monitor clinical trial sites for compliance
• Liaise between investigators and the study team




• Train site staff on study protocols
• Conduct routine visits and assessments
• Manage and resolve study-related issues

Requirements:
• Bachelor's degree in Life Sciences or similar
• At least 3 years of relevant monitoring experience
• Preferred background in Oncology or Infectious Diseases
• Fluent in English
• Significant travel commitment (60-80%)

Contribute to Pfizer's mission of quality patient care through your role as a Senior Clinical Research Associate I.
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📌 Senior Associate for Clinical Research at Pfizer (Manitoba)
🏢 Pfizer
📍 Manitoba