Associate Director, Clinical Quality Management

Kyowa Kirin Pharmaceuticals; Princeton (NJ); On-site; USD 140,000 - 170,000; Full time

Job summary

Kyowa Kirin Pharmaceuticals seeks an Associate Director, Clinical Quality Management to lead quality programs across late-stage trials and regulatory readiness in the U.S. clinical development organization.

Based in Princeton, NJ, the role collaborates with clinical operations, QA and medical affairs to ensure compliance with ICH/GCP, risk-based quality systems, and continuous improvement. The company values scientific rigor and cross-functional leadership.

Job description

Associate Director, Clinical Quality Management

Kyowa Kirin is a fast-growing global specialty pharmaceutical company that applies state-of-the-art biotechnologies to discover and deliver novel medicines in four disease areas: bone and mineral; intractable hematologic; hematology oncology; and rare disease.

Kyowa Kirin Pharmaceutical Development, Inc. (KKD) is a wholly owned subsidiary of Kyowa Kirin USA Holdings, Inc., an industry leader born from the merger of Kyowa Hakko Group and Kirin Group. Backed by six decades of its parent companies’ experience, KKD specializes in the development of new chemical entities and biopharmaceutical therapies. Among other achievements, scientists and collaborators at KKD have leveraged advances in antibody therapeutics to make tremendous strides across key scientific fields, including oncology, immunology and nephrology.

KKD is headquartered in Princeton, New Jersey.