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Job Description & How to Apply Below
Our client seeks a Senior Clinical Research Associate with 4-6 years in pharmaceutical or CRO settings. You will manage clinical site monitoring, support study compliance, and maintain relationships with investigative sites. The position demands strong communication skills and involves travel of up to 75% within Western Canada.
Key Responsibilities:
• Conduct and manage site monitoring activities
• Support site initiation and study closeout visits
• Ensure regulatory compliance and quality standards
• Build strong relationships with investigative sites
• Identify and resolve site issues efficiently
Requirements:
• Bachelor’s degree with 4-6 years CRA experience
• Experience with clinical trials PI-IV monitoring
• Strong knowledge of GCP guidelines
• Excellent organizational and communication skills
• Willingness to travel up to 75% within assigned territory
Make an impact in clinical research through effective monitoring and relationship management.
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Position Requirements
10+ Years
work experience
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