Kyverna Therapeutics is a patient-centered, clinical-stage biopharmaceutical company developing cell therapies for patients with autoimmune diseases. Built on core values—staying true to our mission, accelerating together, clarity first, embracing innovation, and delivering results—we are steadfast in advancing the future of autoimmune disease treatment. Join us to help redefine what’s possible at the forefront of cell therapy innovation.

Kyverna is currently seeking a Medical Communications/Medical Affairs Writer (contract) to develop, coordinate, and execute high-quality scientific publications, conference materials, and other medical content. The role is responsible for communicating clinical and translational data clearly, accurately, effectively, and in a compliant manner. You will work closely with Medical Affairs, Clinical Development, Biostatistics, Regulatory Affairs, and other external writers to ensure data is shared on time and meets global publication standards and company objectives. This is a highly cross-functional role requiring strong scientific writing skills, meticulous attention to detail, and the ability to manage multiple deliverables in a fast-paced clinical environment.

**Job Title:** Medical Affairs Writer (Contract)
**Reports To:** Scientific Director, Medical Affairs
**Location:** Remote
**Contract Term:** 12 months
**Work Hours:** 15–30 hours per week, depending on workload
**Hourly Rate:** $90–$110 per hour

### Responsibilities
– Support the development and execution of global medical communications and publication plans aligned with Medical Affairs and clinical program goals.
– Write, edit, and manage a range of medical communications deliverables, including:
– Manuscripts (primary manuscripts)
– Review articles
– Abstracts
– Slides (for MSLs and HCPs)
– Congress posters and oral presentations
– Plain-language summaries (as applicable)
– Ensure all content is scientifically accurate, balanced in tone, and consistent with source data.
– Translate complex clinical, preclinical, and translational findings into clear, compelling scientific narratives.
– Manage internal review and approval processes, including version control.
– Collaborate with Clinical Development, Biostatistics, Regulatory Affairs, Commercial (as applicable), and external medical writers.
– Support author engagement and manuscript iteration by coordinating feedback and revisions with KOLs.
– Handle inquiries by monitoring the inquiry email and responding to patient and physician questions using approved templates.

### Qualifications
– Advanced degree in a scientific or medical field (PhD, PharmD, MD, or MS with relevant experience).
– 10+ years of medical/scientific writing experience, with a track record of producing publications for biotechnology, pharmaceutical, or medical communications organizations.
– Proven experience writing manuscripts, abstracts, and conference materials.
– Knowledge of clinical trial design, statistics, and data interpretation.
– Familiarity with publication ethics and relevant guidelines (ICMJE, GPP).
– Experience supporting publications related to cell therapy, immunology, and/or rare or autoimmune diseases.
– Strong scientific writing and editing skills.
– Excellent project management and organizational abilities.
– Ability to work independently while collaborating effectively across teams.
– Strong attention to detail and commitment to quality and compliance.
– Clear communication skills and the ability to manage competing priorities.

$90–$110 per hour.