Jobs at Kyverna Therapeutics

The Associate Director will lead SEC reporting, technical accounting, and SOX compliance, ensuring timely filings and guiding cross-functional teams in complex accounting matters.

Lead and build Kyverna's Manufacturing and Supply Chain function for autologous and allogeneic cell therapies. Manage CMOs, vendors, clinical supply, sourcing, logistics, budgets, and regulatory compliance. Develop operational plans, supply orchestration and tracking systems, ensure network readiness for pivotal studies and launches, and recruit and develop a high-performing team.

The Sr. Director, Clinical Scientist leads clinical research for Multiple Sclerosis therapies, overseeing study execution, protocol development, and cross-functional collaboration in a biotech setting.

Lead development and execution of CAR T channel strategy and operations, overseeing 3PL, specialty pharmacy, distribution, state licensing, government pricing support, GTN optimization, partner governance, launch readiness, reporting, and cross-functional coordination to ensure scalable, compliant commercialization.

Lead discovery and early development strategy for next-generation immune cell therapies. Oversee multidisciplinary teams, evaluate and advance in vivo CAR-T and cellular engineering technologies, build external collaborations, prioritize discovery investments, and partner with clinical, regulatory, and business teams to progress candidates from discovery through IND-enabling development.

The VP of Commercial Operations will lead and build commercial infrastructure, manage sales field operations, and oversee analytics for cell therapies targeting autoimmune diseases. They will collaborate with cross-functional teams to ensure effective commercialization and launch of products, while developing a high-performing operations team.

Lead integrated lifecycle strategy for emerging therapeutic platforms from discovery through commercialization. Coordinate cross-functional teams (Research, Clinical, Regulatory, Manufacturing, Quality, Commercial) to drive INDs, pivotal studies, PV/PPQ, launch readiness, and lifecycle expansion. Define development pathways, manufacturing strategies, CDMO partnerships, and commercialization plans to maximize portfolio value and mitigate program risk.

Senior leader accountable for integrated development and commercialization strategy of CAR-T programs. Leads lifecycle governance, cross-functional coordination, portfolio prioritization, regulatory and manufacturing readiness, risk assessment, and executive-level decision-making to advance programs from development through regulatory filings and launch.

The Senior Clinical Research Scientist will design, execute, and analyze clinical studies, ensuring compliance with GCP and regulatory requirements, and collaborate across multiple departments.

The Sr. Director of Business Development will drive Kyverna's growth strategy through strategic partnerships, licensing, and collaboration in the biopharmaceutical sector.