(Senior) Clinical Quality Associate Director - 12 month secondment/fixed term contract

The Clinical Quality Associate Director (CQAD) is primarily responsible for maintaining, developing, and communicating high-quality standards in the delivery of clinical studies. This includes playing a central role in coordinating and meeting the training needs of the local Site Management & Monitoring (SMM) team through close collaboration with local SMM leadership and reporting to Director, Country Head.

This role acts as the primary advisor on compliance and process matters within the local SMM team, proactively identifying and pursuing opportunities to drive quality and process improvements at local, regional, and global 
levels. 
A key aspect of the role is the development, implementation, and continuous oversight of local procedural documents, as well as ensuring up-to-date knowledge of local regulations and industry practices pertaining to clinical trials. The CQAD supports audit and inspection activities, serving as the primary point of contact for audito...