The Manager, Quality Systems will oversee and enhance the quality management systems at Kyverna, ensuring compliance with regulatory standards and fostering a culture of quality. Responsibilities include managing processes for deviations, investigations, CAPAs, and quality metrics while collaborating with Technical Operations and developing training for QMS programs.

The Senior Director of Biostatistics will lead the Biostatistical group at Kyverna Therapeutics, overseeing clinical studies and providing strategic biostatistical guidance. Responsibilities include statistical analysis execution, study design, collaboration with CROs, and regulatory interaction, ensuring the delivery of projects with rigor and quality.

The Sr. Contracts Counsel will draft, revise, negotiate, and manage various contracts, collaborate with senior management, improve business processes, and ensure compliance with company policies. This role requires strong legal knowledge and the ability to communicate risks effectively.

The Senior Manager/Associate Director of Statistical Programming will lead the establishment of the in-house statistical programming function. Responsibilities include overseeing regulatory submissions, ensuring compliance with CDISC standards, managing external CRO work, and delivering statistical programming outputs to support clinical trials.

The Supply Chain Coordinator Contractor will support the Manufacturing team by managing logistics, material movement, and coordinating order management processes for cell therapy materials. Responsibilities include collaborating with various stakeholders, monitoring material movement, and managing procurement orders from initiation to delivery.

The Director of Quality Compliance and Risk Management at Kyverna Therapeutics will lead the establishment and enhancement of quality systems, ensuring regulatory compliance across GxP operations. They will develop a risk-based audit strategy, manage domestic and international audits, and foster collaboration between various departments to create a culture of sustainable compliance, ultimately advancing the company’s clinical development programs.

The Technical Program Lead is responsible for leading the development and implementation of a product technical realization roadmap, managing budgets, ensuring effective communication with stakeholders, and providing strategic direction throughout the Program. The role includes overseeing the CMC development process and ensuring alignment with corporate goals as well as cross-functional team collaboration.