Manager of Regulatory Affairs, Consultant

Kyverna Therapeutics

Remote regions

US

Salary range

$75–$85/hr

Benefits

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Responsibilities:

  • 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

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.

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