Medical Writer Job at Kelly, New Brunswick, NJ

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  • Kelly
  • New Brunswick, NJ

Job Description

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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