Clinical QA manager

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

As a Clinical QA Manager at ICON, you will be is responsible for ensuring robust oversight of clinical trial compliance at the country and site level. This role applies a risk-based approach to proactively identify, evaluate, and manage compliance risks, ensuring adherence to Good Clinical Practice (GCP), company procedures, and regulatory requirements. The role partners closely with country, regional and general stakeholders to safeguard patient safety, data integrity, and inspection readiness.

What You Will Do

Your focus will be on coordinating clinical quality assurance and compliance delivery, resolving issues, and developing team capability.

Key Responsibilities Include





- Developing and implementing quality assurance strategies and processes to support clinical trial activities.
- Conducting quality assessments and audits to ensure compliance with regulatory standards and guidelines.
- Collaborating with project teams to identify and address quality issues and implement corrective actions as needed.
- Providing guidance and support to staff regarding quality assurance policies, procedures, and best practices.
- Contributing to the development and maintenance of quality management systems and documentation.

Your Profile

You will have solid quality assurance and compliance experience, with the ability to manage competing priorities and develop your team.

Required Qualifications And Experience

- Bachelor's degree in a relevant discipline
- Minimum of 5 years of experience in quality assurance within the pharmaceutical, biotechnology, or CRO industry.
<

📌 Clinical QA Manager (España)
🏢 ICON Strategic Solutions
📍 España