Senior Clinical Research Associate at ICON Strategic Solutions overseeing clinical trial monitoring and site management in a sponsor-dedicated model. The role focuses on ensuring protocol adherence, regulatory compliance, and quality across multiple trial sites while mentoring junior staff.
Responsibilities
Monitor clinical trial sites for protocol adherence, regulatory compliance, and GCP standards
Conduct site visits to assess performance, troubleshoot issues, and provide operational support
Collaborate with cross-functional teams on timely data collection and accurate reporting
Train and guide site personnel and junior CRAs on clinical trial best practices
Build and maintain effective relationships with site personnel and stakeholders
Requirements
Bachelor's degree in scientific or healthcare-related discipline
Extensive clinical trial monitoring experience with independent work capability
Demonstrated ability to manage multiple sites and projects concurrently
Expertise in monitoring practices, data integrity, and clinical trial software
Strong stakeholder management and communication skills
Willingness to travel approximately 60% as required
Compensation:
€45,040–€56,300 base

📌 Senior Clinical Research Associate (Milano)
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📍 Milano