19 set - Milano
Icon Clinical
Overview
In this role you will oversee clinical trial activities to ensure protocol alignment, regulatory compliance, and data integrity. You will monitor sites, conduct visits, and collaborate with cross-functional teams to support timely data collection and trial execution. You will train site staff, build strong relationships, and drive high standards of trial conduct. This position offers global exposure and a meaningful opportunity to shape the delivery of clinical development at ICON.
Retribuzione / Benefits
- annual leave entitlements
- health insurance offerings
- retirement planning offerings
- Global Employee Assistance Programme (TELUS Health)
- life assurance
- flexible country-specific optional benefits
Responsabilità
- Monitor trial sites for protocol adherence, regulatory requirements, and GCP standards
- 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 to maintain high trial conduct standards
- Cultivate relationships with site personnel and stakeholders to facilitate smooth trial operations
Requisiti fondamentali
- Advanced degree in life sciences, nursing, or medicine
- Extensive experience as a Clinical Research Associate with strong regulatory knowledge
- Proven ability to manage multiple sites and projects simultaneously with strong organizational skills
- Expertise in monitoring practices, data integrity, and site management
- Proficiency in relevant clinical trial software and tools
- Excellent communication, interpersonal, and stakeholder management skills
- Ability to travel at least 60% of the time and possession of a valid driver’s license
- communication
- interpersonal skills
- stakeholder management
- monitoring practices
- data integrity
- site management
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