Clinical QA manager

As Clinical QA Manager you ensure robust clinical trial compliance oversight at country and site levels using a risk-based approach. You collaborate with country, regional and global stakeholders to safeguard patient safety, data integrity, and inspection readiness. You’ll shape quality assurance strategies, conduct audits, and drive corrective actions while developing the QA team and maintaining documented quality systems. This role combines hands-on QA delivery with people leadership in a mission-driven scientific environment.

• Various annual leave entitlements
• Health insurance offerings to suit family needs
• Competitive retirement planning offerings
• Global Employee Assistance Programme (LifeWorks)
• Life assurance
• Flexible country-specific optional benefits (childcare vouchers, bike schemes, gym discounts, travel passes)
• Develop and implement quality assurance strategies and processes for clinical trial activities
• Conduct quality assessments and audits to verify regulatory compliance
• Collaborate with project teams to identify quality issues and implement corrective actions
• Provide guidance on QA policies, procedures, and best practices to staff
• Contribute to development and maintenance of quality management systems and documentation
• Coordinate clinical quality assurance and compliance delivery and resolve issues; build team capability
• Bachelor's degree in a relevant discipline (minimum 5+ years' QA experience in pharma/biotech/CRO)
• Minimum 5 years of quality assurance experience in pharmaceutical, biotechnology, or CRO industries
• Knowledge of regulatory requirements and guidelines governing clinical trials (ICH-GCP, FDA regulations)
• Strong analytical and problem-solving skills with effective quality issue resolution
• Excellent communication and interpersonal skills; ability to collaborate with cross-functional teams