16 set - Varese
Icon Clinical
Overview
In this role you oversee clinical trial monitoring to ensure adherence to protocol, regulatory standards and GCP, driving quality and continuous improvement. You will lead site visits, collaborate with cross-functional teams and mentor site staff, ensuring smooth trial execution. Your work supports ICON’s mission to bring new medicines to patients faster by maintaining rigorous data integrity and site performance. You will engage with site personnel and stakeholders, influencing compliance and operational excellence. This is a globally-facing role with significant travel and impact across multiple trials.
Retribuzione / Benefits
- Competitive base salary and performance-related incentives
- Health and wellbeing programmes (medical, dental, vision)
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes and wellbeing resources
- Learning and development opportunities and structured career pathways
Responsabilità
- Monitor trial sites for protocol compliance, regulatory adherence, and GCP standards
- Conduct site visits to assess performance, resolve issues, and support successful execution
- Collaborate with cross-functional teams to ensure timely, accurate data collection and reporting
- Provide training and guidance to site staff and other CRAs to maintain high trial conduct standards
- Build and maintain effective relationships with site personnel and stakeholders to facilitate operations
Requisiti fondamentali
- Bachelor in relevant scientific discipline or healthcare-related field
- Extensive experience as a Clinical Research Associate with strong understanding of trial processes and regulatory requirements
- Proven ability to manage multiple sites and projects simultaneously with strong organizational and problem-solving skills
- Expertise in monitoring practices, data integrity, and site management; proficient in relevant clinical trial software and tools
- Excellent communication, interpersonal and
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