About the role
Job | Kyverna Therapeutics Platform & Pipeline Opportunity CAR T-Cell Therapy Pipeline Clinical Trials and Expanded Access Patients Experience Stiff Person Syndrome Myasthenia Gravis Multiple Sclerosis Lupus Nephritis Systemic Sclerosis Inside Kyverna Leadership Mission & Values Education & Events Publications Videos Investors News Careers Contact --> ← Back Executive Director, Regulatory Affairs Remote Regulatory Affairs Full Time The Executive Director, Regulatory Affairs will provide strategic and operational regulatory leadership across Kyverna's cell therapy portfolio, with a focus on commercial readiness, labeling strategy, and health authority engagement. The ideal candidate is a seasoned regulatory leader with deep experience in advanced therapies who can shape regulatory strategy from early development through approval and launch, while partnering closely with Clinical, CMC, Commercial, Market Access, and Legal teams. The Executive Director will define and execute global regulatory strategy to support clinical development, registration, and commercialization of Kyverna's autoimmune cell therapies.
The role requires the ability to translate scientific and clinical data into approvable, commercially viable labeling and to lead interactions with regulatory authorities, including FDA and global counterparts. Title: Executive Director, Regulatory Affairs Location: Remote (West Coast hours preferred) Reports to : SVP, Chief Regulatory Officer
Responsibilities Lead global regulatory strategy for Kyverna's development programs, aligning clinical, CMC, and commercial objectives from early development through post-approval lifecycle management. Provide regulatory input to program governance, asset prioritization, and portfolio decisions, including scenario planning and risk mitigation. Anticipate and address regulatory challenges related to cell therapy development, manufacturing, comparability, and long-term follow-up. Serve as the primary senior regulatory interface with FDA, EMA, and other global health authorities. Lead and/or support key regulatory meetings, including INTERACT, pre-IND, End-of-Phase, pre-BLA/MAA, Advisory Committees, and post-marketing commitments. Drive regulatory negotiation strategy, including benefit-risk, endpoints, comparability, and post-approval