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Job Description & How to Apply Below
Elevate your career with Solomon Page as a Senior Clinical Research Associate. This position involves vital monitoring tasks and regulatory compliance in clinical trials across Western Canada.
The ideal candidate will hold a Bachelor’s degree and possess 4-6 years of relevant CRA experience, particularly in pharmaceutical or CRO settings. Your responsibilities will include site monitoring, compliance with study protocols, and establishing strong site relationships. Organizational and communication proficiency is critical for success.
Key Responsibilities:
• Manage and conduct clinical site monitoring activities
• Support both site initiation and routine monitoring
• Ensure adherence to quality and regulatory standards
• Develop and maintain relationships with investigative sites
• Troubleshoot and address site issues to meet study timelines
Requirements:
• Bachelor’s degree in a related field
• 4-6 years of CRA experience in pharmaceutical or CRO
• Comprehensive understanding of clinical trial regulations
• Effective communication and relationship management skillset
• Ability to travel up to 75% within Western Canada
Contribute your expertise to pivotal clinical research as a Senior Clinical Research Associate with Solomon Page.
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Position Requirements
10+ Years
work experience
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