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Novartis

Expert Scientific Writer

Posted Yesterday
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In-Office
Dublin
Expert/Leader
In-Office
Dublin
Expert/Leader
Lead end-to-end development of high-quality scientific materials (slide decks, congress content, advisory board resources), synthesize complex clinical data into clear messaging, ensure scientific accuracy and governance compliance, and collaborate across global matrix teams to harmonize content and support lifecycle management.
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Job Description Summary

This role is responsible for creating high‑quality, scientifically rigorous content that advances strategic priorities and reinforces a cohesive scientific narrative. You will lead end‑to‑end development of diverse scientific materials, including medical education slide decks, congress and symposia content, advisory board materials, and scientific assets for internal and external engagements, ensuring accuracy, clarity, and first‑time‑right execution.
Experience in one of the following therapeutic areas is required: Oncology, Cardiovascular, Renal, Neuroscience, or Immunology. Candidates will be assigned to work within the therapeutic area that aligns with their expertise. You will collaborate effectively within a global matrix, partnering with Scientific Writers, IMA (IMACE and TAs), Global Medical Affairs, and cross‑functional medical, clinical, and commercial teams. Through these partnerships, you will drive content excellence, uphold governance standards, and ensure alignment across therapeutic areas and markets to support an impactful global scientific communication strategy.
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Job Description

Key Responsibilities:

Scientific Content Development

  • Develop high‑quality, scientifically rigorous materials - including slide decks, congress/symposia content, and advisory board resources - aligned to the overarching scientific narrative. Ensure scientific precision, clarity, and IMACE‑level quality standards across all materials, supporting review processes with strong input on messaging, data accuracy, and consistency.

  • Own end‑to‑end delivery of scientific content, ensuring first‑time‑right execution across multiple concurrent projects and brands.

  • Research, interpret, and synthesize complex scientific and clinical data into clear, accurate, strategically aligned content for diverse audiences.

  • Provide scientific insight to address data‑related queries, support problem solving, and ensure precise messaging.

Matrix Collaboration & Stakeholder Engagement

  • Partner closely with IMA, GMA, and cross‑functional clinical, and commercial teams to understand priorities and refine scientific messages.

  • Integrate feedback efficiently and contribute to publications planning, research activities, and team capability building through mentoring and onboarding.

  • Support continuous improvement of content formats, tools, and delivery approaches across channels and therapeutic areas.

Content Excellence, Governance & Harmonization

  • Uphold scientific quality, accuracy, consistency, and adherence to templates, SOPs, and governance processes, ensuring all content is compliant and audit‑ready.

  • Promote harmonization of scientific communications across therapeutic areas and markets to support an integrated and impactful communications strategy.

  • Apply structured content and digital platforms to maintain, update, and optimize scientific materials, enabling lifecycle management, reuse, and improved efficiency.

Essential Requirements:

  • Education and Experience: Minimum BSc with 10+ years relevant experience, Preferred Advanced degree (PhD/Postdoc/MD) with 5+ years of relevant experience.

  • Extensive experience developing scientific or medical content within pharmaceutical, biotech, or healthcare communications environments.

  • Over 2 years of experience in at least one therapeutic area: Oncology, Cardiovascular, Renal, Neuroscience, or Immunology.

  • Proven ability to interpret, synthesize, and communicate complex scientific and clinical data with high scientific rigor.

  • Strong experience working in global, matrixed, crossfunctional teams (Medical Affairs, Clinical Development, etc.). Demonstrated ability to manage multiple concurrent scientific projects under tight timelines across brands or therapeutic areas.

  • Solid understanding of medical review processes, documentation management, compliance standards, and version control.

  • Proficiency with digital and modular content platforms and structured content approaches.

  • Fluent oral and written English; additional languages desirable.

Benefits & Rewards:

  • Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards

Commitment to Diversity and Inclusion:  

  • Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.

Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture

Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network


 

Skills Desired

Novartis Dublin, Dublin, IRL Office

203 Merrion Rd, Dublin, Ireland, D04 NN12

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