[Hiring] Medical Affairs Writer @Kyverna Therapeutics
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Role Description
This role involves the development, coordination, and execution of high-quality scientific publications, congress materials, and medical content that communicate clinical and translational data accurately, compliantly, and effectively.
• Support the development and execution of the global medical communication and publication plans aligned with Medical Affairs and clinical program objectives
• Author, edit, and manage a range of publication and other medical communication deliverables, including:
• Primary manuscripts
• Review articles
• Abstracts
• Slide Decks (MSL and HCP)
• Congress posters and oral presentations
• Plain language summaries (as applicable)
• Ensure content is scientifically accurate, balanced, and aligned with source data
• Translate complex clinical, preclinical, and translational data into clear, compelling scientific narratives
• Manage internal review, approval workflows, and version control
• Partner with Clinical Development, Biostatistics, Regulatory, Commercial (as appropriate), and external medical writers
• Support author engagement, including coordinating feedback and revisions with key opinion leaders (KOLs)
• Inquiry management – Monitor the inquiry inbox and respond to patient and physician inquiries using approved templates
Qualifications
• Advanced degree in a scientific or medical discipline (PhD, PharmD, MD, or MS with relevant experience)
• 10+ years of medical or scientific writing experience in publications within biotech, pharma, or medical communications
• Demonstrated experience authoring manuscripts, abstracts, and congress materials
• Strong understanding of clinical trial design, statistics, and data interpretation
• Working knowledge of publication ethics and guidelines (ICMJE, GPP)
• Experience supporting publications for cell therapy, immunology, or rare/autoimmune diseases
• Exceptional scientific writing and editing skills
• Strong project management and organizational abilities
• Ability to work independently while collaborating effectively across functions
• High attention to detail and commitment to quality and compliance
• Clear communicator with the ability to manage competing priorities
Requirements
• Hourly rate: $90/hr-$110/hr
• Duration: 12 months, 15-30 hours per week depending on workload
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