Clinical Research Associate
Icon Clinical PLC
forschende pharmazeutische Industrie
Milano - Italien
Senior Fachkraft / Projektleiter
Experteer Overview
As a Senior Clinical Research Associate at ICON Biotech, you will oversee multicenter trial activities to ensure protocol adherence, regulatory compliance, and data integrity. You’ll monitor sites, conduct visits, and collaborate with cross-functional teams to drive accurate data collection and trial execution. You will train site staff and build strong relationships to support smooth operations. This role offers the chance to influence trial quality within a leading biotech-focused CRO and travel across Italy to sites.
Leistungen / Benefits
- Various annual leave entitlements
- Health insurance offerings
- Competitive retirement planning
- Global Employee Assistance Programme (TELUS Health)
- Life assurance
- Flexible country-specific optional benefits
Verantwortungsbereiche
- Monitor trial sites to ensure protocol, regulatory, and GCP compliance
- Conduct site visits to assess performance, resolve issues, and support trial execution
- Collaborate with cross-functional teams to ensure timely data collection and reporting
- Provide training and guidance to site staff and other CRAs
- Build and maintain relationships with site personnel and stakeholders to enable smooth operations
Zentrale Anforderungen
- Advanced degree in life sciences, nursing, or medicine
- Certification (Italian Law)
- Extensive CRA experience with strong knowledge of trial processes and regulations
- Ability to manage multiple sites and projects simultaneously with strong organization and problem-solving skills
- Expertise in monitoring practices, data integrity, and site management; proficiency in clinical trial software and tools
- Excellent communication, interpersonal, and stakeholder management skills; ability to influence and drive compliance in a complex environment
- Ability to travel across Italy as required (car/train/flight)
Stellenbeschreibung
As a Senior Clinical Research Associate at ICON Biotech, you will oversee multicenter trial activities to ensure protocol adherence, regulat…
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