Clinical Research Associate I

Job description

Clinical Research Associate I Drive clinical excellence from protocol to patient – where your monitoring expertise ensures trial quality and patient safety across our global pipeline. Your new role: As a Clinical Research Associate I, you'll provide strategic oversight of clinical trial sites across our global portfolio, ensuring protocol compliance, data integrity, and patient safety. You'll be the vital link between Novo Nordisk, clinical sites, and cross-functional teams, driving study quality through risk-based monitoring and proactive collaboration. This position is a maternity leave cover. Your responsibilities will include: This role requires flexibility to travel as required and is based within our Global Trial Portfolio (GTP), Trial Operations EUCAN. - Serving as the primary liaison between Novo Nordisk, clinical sites, and cross-functional study teams, conducting on-site and offsite monitoring visits in accordance with ICH-GCP, SOPs, 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 regulatory standards - Overseeing site performance, r...