This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for an Associate Director, Clinical Quality Assurance based in the United States. This is an exciting opportunity for an experienced clinical quality professional to lead and strengthen Good Clinical Practice (GCP) quality assurance across clinical development programs, from early to late-stage trials. You will play a key role in ensuring clinical research activities meet global regulatory requirements, international guidelines, and internal quality standards. Working in a collaborative, fast-paced biopharmaceutical environment, you will oversee quality programs, lead risk-based audits, and promote inspection readiness across clinical operations. The role offers broad cross-functional exposure, with opportunities to influence study design, improve compliance processes, and proactively manage quality risks. You will serve as a trusted GCP expert, partnering with clinical teams and external service providers to maintain the highest standards of research integrity. If you are passionate about quality excellence and advancing clinical development, this position offers the opportunity to make a meaningful contribution to patient safety and the delivery of innovative therapies.