Search the 13 jobs at Kyverna Therapeutics

The Senior Manager of Quality Assurance will oversee Contract Manufacturing Organizations (CMOs) to ensure compliance with Good Manufacturing Practices (GMP) and facilitate investigational product release for clinical trials. Responsibilities include batch record reviews, quality system approvals, on-site oversight, and managing relationships within the CMO network.

The Manager, Quality Systems will oversee quality systems activities including Deviations, Investigations, CAPAs, Change Controls, and Quality Metrics. This role requires close collaboration with Technical Operations, ensuring compliance with regulatory standards, and supporting continuous improvement in QMS programs.

The Manager, GxP Training will oversee quality training programs, manage training practices and SOPs, and ensure compliance with QMS. Responsibilities include delivering courses, reporting on training activities, and enhancing training through KPI evaluation and quality metrics preparation.

The Document Management Senior Specialist will manage documentation integrity, security, and compliance within a drug development environment. Responsibilities include overseeing document management systems, ensuring compliance with regulatory standards, supporting audits, training staff, and collaborating with cross-functional teams to enhance document management processes.

The Director of Talent Acquisition at Kyverna Therapeutics will lead the recruitment efforts for hiring and retaining talent, manage the recruitment process, collaborate with leadership and HR, and design employer branding activities. This role requires effective candidate sourcing and maintaining recruitment metrics while ensuring a positive candidate experience.

The Associate Director of Quality Assurance oversees Contract Manufacturing Organizations to support clinical manufacturing, develops internal QA processes, and manages Quality Assurance staff. Responsibilities include establishing Quality Metrics, ensuring compliance with cGMP, and maintaining effective oversight of clinical product quality, ensuring timely issue resolution and robust quality management strategies.

The Associate Director, Strategic Planning, and Operations will drive the development of target product profiles, maintain long-term forecasts, optimize competitive intelligence, and support strategic assessments and compliance requirements in a clinical-stage cell therapy environment.

The Scientist II will support analytical development by designing, performing, and documenting laboratory studies, providing technical expertise in method validation and transfer, and collaborating on in-house testing and regulatory documentation. Responsibilities include drafting procedures, managing sample data, and evaluating novel methodologies for T cell testing.

The Executive Director of PMO will lead Kyverna Therapeutics' Program Management Office, overseeing strategic planning, execution, and management of projects related to cell therapies for autoimmune diseases. They will mentor project managers, ensure effective stakeholder engagement, and implement process improvements while monitoring project performance and governance standards.

The Senior Data Scientist will collaborate across multi-disciplinary teams to build tools for data visualization and analysis, monitor CAR-T development processes, and facilitate QC to ensure product quality. Responsibilities include integrating high-dimensional data, creating dashboards, analyzing data from clinical trials, and driving understanding of mechanisms affecting patient outcomes.

The Senior Director of Biostatistics will lead the Biostatistical group at Kyverna Therapeutics, providing strategic guidance and oversight for clinical studies. Responsibilities include statistical analysis execution, data collection support, management of clinical studies with CROs, regulatory interactions, and cross-functional collaboration to ensure successful trial execution and compliance with standards.

The Senior Statistical Programmer will lead the development and implementation of programming standards for clinical study data analysis. Responsibilities include generating/validating datasets, approving CDISC-compliant datasets, managing timelines with CROs, and collaborating with teams on documentation and regulatory submissions.

The Translational Scientist will partner with stakeholders to assess clinical metrics, develop data analytical tools, and provide statistical guidance in biomarker strategies for drug development. Responsibilities include innovative statistical analyses of complex data, development of predictive models, and communication with scientific communities.