Clinical Research Associate

Job description

Clinical Research Associate (CRA) Belgium Be the vital link between groundbreaking science and the patients who need it most – safeguarding quality, ensuring compliance, and building the relationships that bring life-changing treatments to life. Your new role: As a Clinical Research Associate, you'll provide strategic oversight and management of clinical trial sites, ensuring every study meets the highest standards of protocol compliance, data integrity, and patient safety. You'll be the trusted partner that sites rely on, driving study quality and performance through proactive risk management and risk-based monitoring. Your day-to-day responsibilities will include: - Serving as the primary liaison between Novo Nordisk, clinical sites, and cross-functional study teams, conducting on-site and remote monitoring visits in accordance with ICH-GCP and regulatory requirements - Ensuring patient safety and data integrity by monitoring site data, resolving discrepancies, and managing adverse events in full compliance with protocols and regulations - Building and maintaining strong relationships with investigators and site staff, providing continuous training and support on study protocols,...