The position

 As a Clinical Research Associate at Novo Nordisk, you will: Oversee and manage assigned clinical trial sites, conducting on-site and remote monitoring visits to ensure compliance with protocols, ICH-GCP guidelines, and regulatory requirements.Drive the implementation of Risk-Based Quality Management (RBQM) principles to proactively identify, assess, and mitigate risks throughout study conduct.Build and maintain strong relationships with investigators, site staff, and cross-functional teams to support efficient clinical trial execution.Monitor site performance, recruitment progress, retention, and data collection to ensure study timelines and quality objectives are met.Ensure patient safety and data integrity by resolving discrepancies, managing adverse events, and maintaining inspection readiness.Provide site training and continuous support on study protocols, operational procedures, systems, and compliance requirements.Act as an ambassador for Novo No...