Novo Nordisk A/S is seeking a Clinical Research Associate to oversee trials across assigned sites, ensuring safety, quality and on-time data delivery. You will monitor sites in office and remotely, apply RBQM principles and manage risks to keep studies on track.
The role requires 1+ year in clinical trial monitoring, robust ICH-GCP knowledge, and the ability to travel up to 70%. You will collaborate with investigators and cross-functional teams to ensure compliant, high-quality trial conduct.
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📌 Clinical Trials Monitor: Site Oversight & Rbqm British Columbia (Canada)
🏢 Novo Nordisk A/S
📍 Canada
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