Medical Writer
Kelly in Partnership with Johnson & Johnson is hiring for a Medical Writing Specialist
Description:
The Medical Writing Specialist supports the development, review, and dissemination of scientific materials for payers, healthcare intermediaries, and health systems across the assigned J&J IM portfolio. The role focuses on delivering high-quality, evidence-based, and compliant scientific content, including standard and custom materials, metrics reporting, and support for payer-related projects and research. This position works within cross-functional medical teams and reports to the Associate Director/Director, Med Info–PHS, ensuring scientific rigor, regulatory compliance, and timely execution of deliverables.
Key responsibilities include, but are not limited to:
Developing and supporting the timely dissemination of tailored, evidence-based payer scientific materials
Participating in multidisciplinary review teams for regulated payer content
Collaborating with Medical Affairs and Real-World Value & Evidence teams on AMCP dossiers, Medicaid formulary requests, and custom materials
Supporting the development of payer digital assets in partnership with Digital teams
Guiding the creation and delivery of scientific responses to payers and health systems
Supporting delivery of scientific information to Clinical Decision Resource Organizations
Collaborating on drug compendia strategies and interactions
Overseeing vendor deliverables and providing feedback to ensure quality and compliance
Leveraging metrics and voice-of-customer insights to improve content and processes
Participating in ad-hoc projects and research as needed
Required Skills and Experience:
Experience in medical writing within pharmaceutical, clinical, or scientific environments
Strong understanding of scientific content development and regulatory requirements for payer and health system communications
Ability to collaborate effectively in multidisciplinary, cross-functional teams
Strong communication, analytical, and organizational skills
2–3 years of relevant medical writing experience
PharmD degree
Preferred Skills and Experience:
Experience in Oncology, Neuroscience, or Immunology therapeutic areas
Experience supporting development and review of payer scientific content such as AMCP dossiers
Background supporting Medical Affairs and Real-World Value & Evidence projects
Experience interacting with Clinical Decision Resource Organizations or drug compendia
Familiarity with scientific content management systems and regulatory submission platforms
Experience with digital asset development tools and data vendors
Strong project management skills and ability to meet tight deadlines with high-quality outputs
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