Clinical Quality Associate Director

Role Summary

The Clinical Quality Associate Director (CQAD) is responsible for maintaining, developing, and communicating high‑quality standards in the delivery of clinical studies. The CQAD plays a central role in coordinating and meeting the training needs of the local Site Management & Monitoring (SMM) team, advising on compliance and process matters, and driving quality and process improvements at local, regional, and global levels.

Responsibilities

• Advise local study teams on AstraZeneca procedural frameworks, international guidelines such as ICH‑GCP, industry standards, and relevant local regulations.
• Provide accurate and timely updates on local clinical trial regulations, ensuring teams are aware of any changes affecting compliance.
• Support local management in planning and executing Quality Control (QC) activities as outlined in the local QC plan.
• Offer expert guidance and support to local management in ...