Senior CRA

Senior Clinical Research Associate role at ICON overseeing clinical trial activities and site management in a sponsor-dedicated model. Responsibilities include protocol monitoring, site visits, data integrity assurance, and training of site personnel to maintain compliance with regulatory standards and GCP requirements.

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 data collection and reporting
• Train and guide site staff and other CRAs on clinical trial conduct standards
• Build and maintain effective relationships with site personnel and stakeholders

Requirements

• Advanced degree in life sciences, nursing, or medicine
• Extensive experience as Clinical Research Associate with strong trial process knowledge
• Demonstrated ability to manage multiple sites and projects concurrently
• Expertise in monitoring practices, data integrity, and site management
• Strong communication and stakeholder management skills
• Willingness to travel 60% of time; valid driver's license required