Associate Director, Clinical Risk Management
This role involves leading clinical risk management across multiple therapeutic areas, focusing on identifying, assessing, and mitigating quality risks in clinical trials to ensure patient safety, data integrity, and regulatory compliance. The individual will drive risk-based oversight, support inspection readiness, lead quality investigations, and advise on CAPA plans in a global, cross-functional environment. Key activities include coaching teams, maintaining clinical quality plans, and contributing to governance forums to uphold high standards in clinical development.