Drive change as a Clinical Research Associate at Parexel where patient safety and site success are paramount. Here, your contribution enhances clinical trial quality through creative solutions.
In the role of Clinical Research Associate, you'll serve as the primary contact for clinical sites, ensuring they meet enrollment timelines and comply with regulatory standards. Your experience will guide qualification and monitoring visits, while world-class training and reduced travel demands support your career growth and personal development.
Key Responsibilities:
• Conduct site initiation and monitoring visits effectively
• Build rapport to enhance site collaboration and problem-solving
• Safeguard participant rights through rigorous performance reviews




• Develop strategies for timely patient recruitment
• Maintain regulatory documentation and data quality
Requirements:
• Bachelor’s degree in a health-related discipline
• Minimum 18 months direct monitoring experience
• Solid interpersonal and communication skills
• Self-motivated with a versatile work ethic
• Knowledgeable in Clinical Trial Management Systems
Make a significant impact in clinical research at Parexel by fostering collaboration and ensuring high-quality trial standards.
J-18808-Ljbffr

📌 Clinical Research Associate Position At Parexel Quebec City
🏢 Parexel
📍 Quebec City