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Kyverna Therapeutics
Kyverna Therapeutics
5 open remote positions
Kyverna Therapeutics is a patient-centered, clinical-stage biopharmaceutical company developing cell therapies for autoimmune diseases. The company is guided by core values and committed to transforming treatment for autoimmune disease, fostering a culture of ethics and integrity.
Salary Distribution
5 of 5 jobs
Benefits Overview
2 of 5 jobs
Bonus
(2)
Stock Plan
(2)
Benefits
(1)
Open Positions
Develop and lead the enterprise compliance program strategy and roadmap. Serve as program manager for compliance buildout and commercialization-readiness initiatives. Provide practical guidance on healthcare compliance risks related to commercialization.
Compliance
Regulatory
Program Management
Leadership
Administer vendor onboarding and maintenance, including collection and validation of banking information and tax documentation. Serve as primary point of contact for vendor inquiries via phone and email; own escalations end-to-end. Prepare and reconcile AP aging reports and vendor statements, resolving aged/outstanding items.
Coupa
Accounts Payable
Microsoft Excel
Procure-to-Pay
Develop and execute a global training strategy tailored to cell therapy programs across clinical and commercial stages. Build role-specific onboarding, certification, and continuous learning pathways for Medical and Commercial field teams. Deliver comprehensive training including disease state education, CAR T product design, clinical data, safety monitoring, and competitive landscape.
Cell Therapy
Medical Affairs
Training Strategy
Regulatory Compliance
Cross-functional Collaboration
Lead integrated asset strategy across the full lifecycle, including research, clinical development, and commercialization. Drive strategic planning for emerging therapeutic platform technologies and evaluate portfolio opportunities. Ensure alignment across Clinical Development, Manufacturing, Quality, Regulatory, and Commercial teams for late-stage development and launch planning.
Drug Development
Clinical Development
Regulatory Affairs
Strategic Planning
Cross-functional Leadership
Lead operational execution of cell therapy trials from startup through close-out, managing timelines, budgets, and vendor oversight. Ensure compliance with regulatory standards including FDA, EMA, and ICH-GCP, and contribute to protocol development and study documents. Collaborate cross-functionally with clinical operations, data management, regulatory, and manufacturing teams to drive study success.
Clinical Operations
Cell Therapy
Regulatory Compliance
Vendor Management
Cross-functional Leadership