Kyverna Therapeutics is a clinical-stage cell therapy company with the mission of engineering a new class of therapies for autoimmune diseases. The Kyverna therapeutic platform combines advanced T cell engineering and synthetic biology technologies to suppress and eliminate the 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 help transform how autoimmune diseases are treated.
The Director of Medical Writing will be a key member of our Kyverna team responsible for leading and overseeing all medical writing activities across our portfolio of programs. This role, reporting to the Executive Director of Regulatory Operations, will require strategic thinking, strong leadership skills, and a deep understanding of medical writing best practices to ensure the preparation of high-quality clinical, nonclinical, and regulatory and submission documents.
Responsibilities:
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