Sr. CRA in Franckfurt, Deutschland

Senior Clinical Research Associate position at ICON overseeing clinical trial monitoring and site management. Leads technical monitoring activities ensuring protocol adherence, regulatory compliance, and quality standards across multiple sites in a sponsor-dedicated model.

Responsibilities

• Monitor clinical trial sites for protocol adherence, regulatory compliance, and GCP standard maintenance
• Conduct site visits to evaluate performance, resolve issues, and provide operational support
• Collaborate with cross-functional teams on timely and accurate data collection and reporting
• Train and guide site staff and other CRAs on clinical trial conduct standards
• Develop and maintain effective relationships with site personnel and stakeholders

Requirements

• Bachelor's degree in scientific or healthcare-related discipline
• Extensive clinical research associate experience with deep knowledge of trial processes and regulations
• Demonstrated ability to manage multiple sites and projects concurrently
• Proficiency in monitoring practices, data integrity, site management, and clinical trial software
• Fluent in German and English
• Strong organizational, problem-solving, and stakeholder management capabilities
• Willingness to travel approximately 60%