06 ott - Milano
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This role oversees clinical trial operations across multiple sites in Milan, ensuring compliance with study protocols, regulatory standards, and Good Clinical Practice guidelines. The Senior CRA will monitor site performance, coordinate data collection, and provide training to staff while managing stakeholder relationships. The position requires an advanced degree in life sciences or a related field, extensive CRA experience, and willingness to travel internationally at least 60% of the time.
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
Coordinate with cross-functional teams on timely and accurate data collection and reporting
Train site staff and other CRAs on clinical trial conduct standards and best practices
Maintain relationships with site personnel and stakeholders to facilitate trial operations
Requirements
Advanced degree in life sciences, nursing, medicine, or related field
Extensive clinical research associate experience with clinical trial process knowledge
Ability to manage multiple sites and projects simultaneously
Expertise in monitoring practices, data integrity, and site management
Proficiency with clinical trial software and relevant tools
Strong communication and stakeholder management capabilities
Valid driver's license and willingness to travel 60% domestically and internationally
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