Medical Affairs Writer - Contract

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This range is provided by Kyverna Therapeutics. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range
$90.00/hr - $110.00/hr

Kyverna Therapeutics is a patient-centered, clinical-stage biopharmaceutical company developing cell therapies for patients suffering from autoimmune diseases. Guided by our core values,

Stay True to Why, Collaborate to Accelerate, Lead with Clarity, Boldly Innovative, and Own the Outcome , we are committed to transforming the future of treatment for autoimmune disease. Join us at the forefront of cell therapy innovation and help redefine what’s possible.

Kyverna is seeking a

Medical Communications Medical Affairs Writer (Contract)

responsible for 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. This role partners closely with Medical Affairs, Clinical Development, Biostatistics, Regulatory, and other external writers to ensure timely dissemination of data in accordance with global publication standards and company objectives.

This is a highly cross-functional role requiring strong scientific writing expertise, attention to detail, and the ability to manage multiple deliverables in a fast-paced clinical-stage environment.

Title:

Medical Affairs Writer - Contract

Reports to:

Scientific Director, Medical Affairs

Location:

Remote

Duration:

12 months. 15-30 hours per week depending on workload

Hourly rate:

$90/hr-$110/hr

Responsibilities

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 skillsStrong 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

Seniority level
Not Applicable

Employment type
Contract

Job function
Marketing, Public Relations, and Writing/Editing

Industries
Biotechnology Research, Research Services, and Pharmaceutical Manufacturing

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