Clinical Research Associate

Job description

Drive clinical excellence across trial sites, ensuring the highest standards of patient safety, data integrity, and regulatory compliance in studies that advance treatments for serious chronic diseases. Your new role: As a Clinical Research Associate, you'll be the vital link between Novo Nordisk, clinical sites, and cross-functional teams, driving excellence in trial execution. Your day-to-day responsibilities will include: - Serving as the primary liaison between Novo Nordisk, clinical sites, and study teams, conducting on-site and remote monitoring visits to ensure protocol compliance - Safeguarding patient safety and data integrity by monitoring site data, resolving discrepancies, and managing adverse events in line with ICH-GCP and regulatory requirements - Building and maintaining strong relationships with investigators and site staff to support recruitment, retention, and overall site performance - Driving the implementation of risk-based quality management (RBQM) principles to proactively identify and mitigate risks throughout the study - Overseeing investigational medicinal products, study supplies, essential documents, and equipment to ensure proper accountability and com...