Novo Nordisk is seeking a Clinical Research Associate to ensure quality, compliance and patient safety across assigned sites. You will monitor progress, identify risks early and help sites deliver reliable data on time, acting as a key link between Novo Nordisk and investigators.
The role requires a Life Sciences degree, 1+ year in trial monitoring, solid ICH-GCP knowledge, and proficiency with EDC/CTMS/eTMF. Travel up to 70% and a focus on RBQM are expected.
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📌 Clinical Trials Monitor | RBQM & Site Partner (Southern Grampians Shire)
🏢 Novo Nordisk
📍 Southern Grampians Shire
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