Associate Dir. Cross TA Risk Management
This role involves leading clinical risk management across therapeutic areas, ensuring data integrity, patient safety, and regulatory compliance in global clinical trials. The Associate Director drives risk-based oversight, inspection readiness, and quality governance, working closely with cross-functional teams to identify, assess, and mitigate risks throughout trial lifecycles. They also support audits, inspections, and the development of corrective actions, contributing to a robust quality framework in R&D.