Manager of Regulatory Affairs, Consultant

Kyverna Therapeutics is a patient-centered, clinical-stage biopharmaceutical company focused on developing cell therapies for patients suffering from autoimmune diseases. The Kyverna therapeutic platform leverages advanced T cell engineering to suppress and eliminate autoreactive immune cells at the origin of autoimmune and inflammatory diseases. Be at the forefront of cell therapy innovation by joining scientists, industry veterans and healthcare visionaries and helping transform how autoimmune diseases are treated. Kyverna is seeking an experienced and driven Manager of Regulatory Affairs to join our regulatory team in a Contract position. This role is pivotal in shaping and executing regulatory strategies for our innovative therapies. We are looking for candidates with a proven track record in Clinical/Nonclinical Regulatory Affairs within the biotechnology or pharmaceutical sector. Title: Manager of Regulatory Affairs, Consultant Reports to: Executive Director, Regulatory Affairs Location: Remote (West Coast hours preferred) Duration: Six months Hours: 40/hrs per week Hourly rate: $75 to $85/hr Responsibilities Regulatory Strategy: Contribute to the development and execution of regulatory strategies aligned with corporate objectives and timelines. Assist in planning and coordinating regulatory submissions and interactions with health authorities. Regulatory Submissions: Manage the preparation, review, and submission of all components of regulatory submissions including IN