Join Parexel as a Senior Clinical Research Associate and make a difference in clinical trials. Your expertise will play a vital role in ensuring successful site management and patient welfare.

As you take on the Senior CRA position at Parexel, you will utilize advanced training to conduct monitoring visits and manage site relationships effectively. With a focus on patient safety and trial quality, the role offers the opportunity to work across multiple therapeutic areas while ensuring compliance with all protocols.

Key Responsibilities:
• Execute qualification, initiation, and monitoring visits
• Develop relationships with clinical site staff to resolve issues
• Ensure participant rights are prioritized during trials




• Implement recruitment strategies to meet timelines
• Verify regulatory documentation and trial data integrity

Requirements:
• Over 18 months monitoring experience in clinical research
• Bachelor’s degree in relevant biological science
• Excellent communication skills in English and French
• Independent, productive work style with urgency
• Competency in MS Office and Clinical Trial Systems

Join Parexel’s committed team and contribute to advancing treatments that improve patient lives.
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📌 Senior CRA Role at Parexel (Quebec City)
🏢 Parexel
📍 Quebec City