Senior Clinical Research Associate at ICON overseeing clinical trial monitoring and site management. The role involves ensuring protocol adherence, regulatory compliance, and quality standards while leading technical monitoring tasks and mentoring other team members.
Responsibilities
Monitor clinical trial sites for protocol adherence, regulatory compliance, and GCP standards
Conduct site visits to assess performance, identify issues, and provide operational support
Collaborate with cross-functional teams on accurate data collection and reporting
Train site staff and junior CRAs on clinical trial conduct standards
Build and maintain relationships with site personnel to support trial execution
Requirements
Bachelor's degree in scientific or healthcare-related field
Extensive clinical research associate experience with proven trial process knowledge
Ability to manage multiple sites and projects with strong organizational skills
Expertise in monitoring practices, data integrity, and clinical trial software
Excellent communication and stakeholder management capabilities
Willingness to travel approximately 60% of the time
Compensation:
€45,040–€56,300 base

📌 Senior Clinical Research Associate (Milano)
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📍 Milano