Sr. CRA

In this role you oversee clinical trial monitoring to ensure protocol compliance, regulatory adherence, and GCP standards. You work with cross-functional teams to ensure timely data capture and effective site support, driving quality and continuous improvement. You train site staff and CRA colleagues to uphold high conduct standards and build strong site relationships to enable smooth trial execution. This position fits ICON’s mission of delivering new medicines faster by elevating trial quality and collaboration. You will engage across sites to manage multiple trials and travel as needed to ensure site performance and regulatory compliance.

• Competitive base salary
• Performance related incentives
• Health and wellbeing programmes
• Retirement and pension plans
• Life assurance and disability coverage
• Learning and development opportunities

• Monitor clinical trial sites for protocol and GCP compliance
• Conduct site visits to assess performance and resolve issues
• Collaborate with cross-functional teams for timely data collection and reporting
• Provide training and guidance to site staff and CRAs
• Build and maintain relationships with site personnel and stakeholders

• Bachelor's degree in a relevant scientific discipline or healthcare-related field
• Extensive experience as a Clinical Research Associate with strong understanding of trial processes and regulatory requirements
• Ability to manage multiple sites and projects with strong organizational and problem-solving skills
• Expertise in monitoring practices, data integrity, and site management; proficiency with clinical trial software and tools
• Excellent communication, interpersonal, and stakeholder management skills; ability to influence and drive compliance in a complex environment
• Fluent in German and English
• Willingness to travel approximately 60%

• strong communication
• stakeholder management
• problem-solving
• monitoring practices
• data integrity
• site management