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Responsibilities:
- Lead global publication strategy development and lifecycle management for Kyverna’s therapeutic pipeline.
- Drive execution of scientific publications, including manuscripts and congress materials, ensuring quality and compliance.
- Facilitate cross-functional Publication Team meetings with Clinical Development, Biostatistics, and Regulatory stakeholders.
Qualifications:
- Advanced degree (PhD, PharmD, MD, or equivalent) in a scientific or health-related field preferred.
- 7+ years of experience in medical communications within biotech, pharmaceutical, or medical communications environments.
- Deep understanding of clinical trial design, data interpretation, and GPP/ICMJE compliance requirements.
Additional Details:
- This role requires strategic leadership and hands-on execution in a fast-paced environment.
- Willingness to travel up to approximately 20% for key scientific congresses and external engagements.
- CMPP certification is preferred for this position.
Kyverna Therapeutics
Kyverna Therapeutics is a patient-centered, clinical-stage biopharmaceutical company developing cell therapies for patients suffering from autoimmune diseases. Guided by core values like collaboration, innovation, and ownership, the company is at the forefront of cell therapy innovation, aiming to transform the future of autoimmune disease treatment.