Experteer Overview

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In this role you ensure robust clinical quality assurance oversight across country and site levels, applying a risk-based approach to identify and manage compliance risks. You will partner with global, regional and country stakeholders to safeguard patient safety, data integrity, and inspection readiness. You lead QA strategies, drive audits, and guide teams to uphold GCP and regulatory standards. This position offers meaningful impact in shaping compliant, patient-centric clinical development at ICON.

Compensaciones / Beneficios
• Develop and implement quality assurance strategies to support clinical trial activities
• Conduct quality assessments and audits to ensure regulatory compliance
• Collaborate with project teams to identify quality issues and implement corrective actions




• Provide guidance and training on QA policies, procedures, and best practices
• Contribute to development and maintenance of quality management systems and documentation

Responsabilidades
• Bachelor's degree in a relevant discipline
• Minimum 5 years of quality assurance experience in pharma, biotechnology, or CRO
• Knowledge of ICH-GCP and FDA regulations
• Strong analytical xqbhyrx and problem-solving skills
• Excellent communication and interpersonal abilities for cross-functional collaboration
• Willingness to travel (~35%)

Requisitos principales
• Various annual leave entitlements
• Health insurance offerings
• Competitive retirement planning
• General Employee Assistance Programme LifeWorks
• Life assurance
• Flexible country-specific optional benefits

📌 Clinical QA Manager (Barcelona)
🏢 Icon Clinical
📍 Barcelona