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Clinical Operations Coordinator
Job Description & How to Apply Below
Elevate clinical research at Nexa Trials as a Clinical Research Coordinator in Markham, Ontario. This hybrid role plays a critical part in enhancing data accuracy and workflow efficiency.
Nexa Trials is looking for a detail-oriented Clinical Research Coordinator to liaise between research sites and operational teams. You will train site staff on Nexa Source technologies, monitor study compliance, and ensure high-quality data collection. Your hands-on approach will foster strong collaborations with principal investigators and address operational challenges effectively.
Key Responsibilities:
• Train coordinators on Nexa Source forms and workflows
• Collaborate with PIs to confirm study protocols
• Monitor overdue assessments and document gaps
• Ensure effective eSource-to-EDC processes with QC teams
• Conduct GCP documentation training sessions
Requirements:
• 3–5 years’ experience in clinical research settings
• Knowledge of ICH-GCP regulations
• Experience with eSource and EDC systems
• Strong organizational skills for multiple studies
• Excellent communication skills for teams
Drive operational excellence and clinical data integrity at Nexa Trials in this pivotal coordinator role.
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