Clinical Research Associate 3

Experteer Overview

You’ll train site staff and build strong relationships with study sites and stakeholders. The position combines independent work with guidance to others, contributing to ICON’s mission to advance clinical development. A meaningful hook is your ability to elevate trial quality and process improvements at scale.

• Monitor sites to ensure adherence to study protocol, regulatory requirements, and GCP standards
• Conduct site visits to assess performance, resolve issues, and support successful trial execution
• Collaborate with cross-functional teams to ensure timely and accurate data collection and reporting
• Provide training and guidance to site staff and fellow CRAs to uphold high conduct standards
• Build and maintain effective relationships with site personnel and stakeholders to enable smooth trial operations

• 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 simultaneously with strong organizational and problem-solving skills
• Expertise in monitoring practices, data integrity, and site management with proficiency in relevant clinical trial software and tools
• Excellent communication, interpersonal, and stakeholder management skills with ability to influence and drive compliance in a complex environment
• Willingness to travel approximately 60%

• Annual leave entitlements
• Health insurance offerings
• Competitive retirement planning
• Global Employee Assistance Programme (LifeWorks) with 24-hour access to professionals
• Life assurance
• Flexible country-specific optional benefits such as childcare vouchers, bike purchase schemes, discounted gym memberships, travel support