Clinical research associate 2
Pubblicato il 01-08-2026 - Experteer Italy in Italia
Experteer Overview In this role you will provide strategic oversight of clinical trial sites to ensure protocol adherence, patient safety, and high-quality data. You will drive study quality through risk-based monitoring and collaborate with investigators and cross-functional teams. Your work supports the execution of trials across obesity, diabetes and other chronic diseases within Novo Nordisk's Global Trial Portfolio. You'll focus on maintaining compliance, managing risks, and accelerating patient access to innovative therapies. Benefits Act as Site Manager to build trusted partnerships with investigators and site staff and ensure high-quality trial execution Conduct on-site and remote visits (site selection, initiation, monitoring, close-out) per Monitoring Plan, Protocol, ICH-GCP and SOPs Implement Risk-Based Quality Management (RBQM) to identify and mitigate risks during study conduct Oversee site performance, recruitment, retention,
and data collection to meet timelines and quality objectives Lead site training and provide ongoing support on study protocols, systems, and compliance Manage IMP, study supplies, essential documents and the Investigator Trial Master File for accountability and compliance Responsabilità Bachelor in Life Sciences Minimum 3 years of clinical trial monitoring experience in pharma or CRO Proven independence in monitoring and strong ICH-GCP E6(R3) knowledge GCP certification (valid) Solid knowledge of CTMS, EDC, IWRS and e TMF Digital mindset with willingness to leverage AI tools for monitoring and data quality Excellent stakeholder management, communication and negotiation skills Fluency in Italian and English; willingness to travel monthly Requisiti fondamentali Continuous learning Career development Incentives and salary competitiveness Global company culture Benefits tailored to life and career stage Monthly travel readiness #J-18808-Ljbffr