Descrizione:
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 eTMF
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
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