As Clinical QA Manager at ICON, you oversee clinical trial quality and compliance at country and site levels using a risk-based approach. You partner with country, regional, and global stakeholders to protect patient safety, data integrity, and inspection readiness. You'll design QA strategies, lead audits, and drive corrective actions while developing the QA team.

This role connects regulatory compliance with everyday trial work in a values-driven environment. It offers meaningful impact by strengthening QMS and cross-functional collaboration.

Competitive base salary and incentives

Health and wellbeing programmes

Retirement and pension plans

Life assurance and disability coverage

Employee assistance programmes and wellbeing resources

Learning and development opportunities

Develop and implement quality assurance strategies and processes for 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 on QA policies, procedures and best practices

Contribute to development and maintenance of quality management systems and documentation

Bachelor's degree in a relevant discipline

Minimum of 5 years' QA experience in pharmaceutical, biotechnology, or CRO

Knowledge of regulatory requirements (ICH-GCP, FDA regulations)

Strong analytical and problem-solving skills

Excellent communication and interpersonal skills with cross-functional collaboration

Willingness to travel ~35%

Legal right to work in the country of employment

📌 Clinical QA manager (Milano)
🏢 Altro
📍 Milano