ICON seeks a Senior Clinical Research Associate to oversee clinical trial monitoring and site management across UK locations. The role involves ensuring protocol adherence, regulatory compliance, and data integrity while leading cross-functional teams and mentoring junior staff.

Responsibilities

• Monitor clinical trial sites for adherence to protocols, regulatory requirements, and GCP standards
• Conduct site visits to assess 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 junior CRAs to maintain clinical trial conduct standards
• Build and sustain relationships with site personnel and stakeholders to facilitate trial operations

Requirements

• Bachelor's degree in scientific or healthcare-related field
• Extensive clinical research associate experience with deep knowledge of trial processes and regulations
• Proven ability to manage multiple sites and projects concurrently
• Expertise in monitoring practices, data integrity, and clinical trial software
• Strong English communication and stakeholder management skills
• Valid driving licence and willingness to travel domestically