Manager of Regulatory Affairs, Consultant; Fully Remote

• Contribute to the development and execution of regulatory strategies aligned with corporate objectives.
• Assist in planning and coordinating regulatory submissions and health authority interactions.
• Prepare and coordinate responses to queries from health authorities.

Requirements:

• Bachelor's or advanced degree in a relevant scientific field.
• Minimum of 2-5+ years in Regulatory Affairs within biotech or pharma.
• Experience with cell or gene therapy regulatory affairs and CTD/eCTD.

About Kyverna:

• Patient-centered, clinical-stage biopharmaceutical company developing cell therapies.
• Focus on transforming treatment of autoimmune diseases through advanced T cell engineering.

Kyverna Therapeutics is a patient-centered, clinical-stage biopharmaceutical company focused on developing cell therapies for autoimmune diseases. It leverages advanced T cell engineering to suppress and eliminate autoreactive immune cells, with a culture driven by scientists and industry veterans.

We are currently recruiting a Manager of Regulatory Affairs, Consultant (Fully Remote) for our team in United States.