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Job Description & How to Apply Below
Location: Warman
Join Fortrea as a Senior Clinical Research Associate specializing in cardiac studies, with significant monitoring responsibilities across Canada. This role includes essential travel during study start-up and execution.
Candidates should have complex cardiac experience, preferably in electrophysiology or medical devices, along with 3+ years of monitoring experience. You will oversee site management, ensuring compliance with SOPs and regulatory requirements while managing project timelines and expectations. Your skills will directly impact the success of clinical trials.
Key Responsibilities:
• Lead clinical site monitoring and manage study files
• Conduct pre-study, initiation, and closeout visits
• Monitor case report data and maintain audit readiness
• Serve as Local Project Coordinator for assigned protocols
• Assist in clinical trial report writing and development
Requirements:
• 3 years of experience in clinical monitoring
• Relevant degree or certification in life sciences
• Excellent planning and organizational skills
• Strong communication skills in English
• Ability to work independently with minimal supervision
Take the next step in your career at Fortrea by utilizing your cardiac expertise in vital clinical trials.
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Position Requirements
10+ Years
work experience
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