Clinical Research Associate

Job description

LOCATION: Porto area preferred. Candidates based in Lisbon can also be considered Are you passionate about clinical research and improving patients' lives? Do you thrive in a fast-paced environment where quality, agility and collaboration matter? If you want to be part of a team delivering clinical trials that make a real difference, this could be your next role. Your new role: As a Clinical Research Associate (CRA), you will be responsible for end-to-end site management and monitoring activities in Phase II–III clinical trials, ensuring compliance with ICH-GCP, protocol requirements, and Novo Nordisk procedures — while maintaining a strong focus on quality, timelines, recruitment and patient protection. In this role, you will: - Serving as the primary liaison between Novo Nordisk, clinical sites, and study teams, con-ducting on-site and remote monitoring visits to ensure protocol compliance - Manage sites across the trial lifecycle (selection, initiation, conduct and close-out), driving inspection readiness and high-quality documentation - Build strong, trusted partnerships with new and existing sites, acting as an ambassador for Novo Nordisk and supporting site performance - Appl...