Drive clinical trial success with ICON plc as a Senior Clinical Research Associate. Focus on site management, team development, and ensuring data integrity in a collaborative environment.

ICON is a leader in healthcare intelligence and clinical research, seeking a Sr. CRA to enhance clinical trial monitoring. You will lead site management activities, manage site queries, and ensure compliance with regulatory guidelines. Your expertise will guide CRAs, contributing to both their growth and study success.

Key Responsibilities:
• Lead site selection, initiation, and monitoring activities
• Act as the primary contact for clinical sites and resolve issues
• Verify data integrity through thorough monitoring and verification
• Mentor CRAs and ensure best practices in studies
• Collaborate with cross-functional teams for trial success

Requirements:
• Bachelor's degree in a scientific or healthcare field
• Fluent i...