Opportunity Description
Drive clinical research innovation as a Senior Clinical Research Associate at Fortrea, focusing on cardiac and medical devices. Leverage your monitoring experience for significant projects across Canada.
You will be responsible for managing site oversight and ensuring adherence to ethical guidelines and regulatory compliance. With your complex cardiac experience, you’ll facilitate study execution from start-up to close-out. Your skills in data review and quality control will play a critical role in advancing clinical trials.
Key Responsibilities:
• Oversee all aspects of site management and monitoring
• Conduct quality control visits and training sessions
• Ensure timely reporting and data integrity
• Review and analyze project progress against targets
• Manage communication with study sites and vendors
Requirements:
• Minimum of three years in clinical monitoring
• Thorough knowledge of regulatory requirements
• Advanced skills in site and registry man...
You will be responsible for managing site oversight and ensuring adherence to ethical guidelines and regulatory compliance. With your complex cardiac experience, you’ll facilitate study execution from start-up to close-out. Your skills in data review and quality control will play a critical role in advancing clinical trials.
Key Responsibilities:
• Oversee all aspects of site management and monitoring
• Conduct quality control visits and training sessions
• Ensure timely reporting and data integrity
• Review and analyze project progress against targets
• Manage communication with study sites and vendors
Requirements:
• Minimum of three years in clinical monitoring
• Thorough knowledge of regulatory requirements
• Advanced skills in site and registry man...
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