Sr. Clinical Research Associate

Experteer Overview

As a Senior CRA at ICON, you oversee clinical trial activities to ensure protocol adherence, regulatory compliance, and data integrity. You will support site visits, train staff, and collaborate with cross-functional teams to drive smooth trial execution. The role is pivotal in safeguarding participant safety and trial quality across sites and studies. You will work within a diverse, inclusive culture that values excellence and impactful clinical development.

Retribuzione / Benefits

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

Responsabilità

• Advanced degree in a relevant field (life sciences, nursing, or medicine)
• Extensive experience as a Clinical Research Associate with strong regulatory knowledge
• Ability to manage multiple sites and projects with organizational and problem‑solving skills
• Expertise in monitoring, data integrity, and site management; proficiency with clinical trial software/tools
• Excellent communication, interpersonal, and stakeholder management skills; capable of driving compliance in a complex environment
• Ability to travel at least 60% with a valid driver's license

Requisiti fondamentali

• annual leave entitlements
• health insurance offerings
• retirement planning options
• Global Employee Assistance Programme LifeWorks
• life assurance
• flexible country‑specific optional benefits