Job Description
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 Astra Zeneca 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 addressing and resolving quality‑specific concerns at the local le...