Senior Scientific Writer II

Job Description Summary

Job Description

Key Responsibilities:

Scientific Content Development

• Develop a broad range of scientific and medical materials including slide decks congress/symposia content advisory board materials and internal medical engagement assets.

• Prepare congressrelated materials such as satellite symposia agendas speaker briefing documents and slide content.

• Research interpret and synthesize complex scientific and clinical data into accurate wellreferenced evidencebased content aligned with TA strategies.

• Ensure scientific precision clarity and IMACElevel quality standards across all materials supporting review processes with strong input on messaging data accuracy and consistency.

• Manage multiple concurrent projects potentially across more than one brand while maintaining high quality and timely delivery.

Matrix Collaboration & Stakeholder Engagement

• Collaborate with functional and cross-functional partners (IMA GMA medical clinical etc.) to align on scientific priorities and clarify content requirements. Participate in routine discussions to refine key messages and ensure content is accurate consistent and fit for purpose.

• Contribute to enhancements in content formats delivery approaches and tools to improve experience and effectiveness across channels.

Quality Standards & Governance

• Ensure all materials comply with internal policies external regulations structured review processes and governance frameworks.

• Apply established templates writing standards QC processes and documentation requirements to maintain scientific rigor quality and auditready outputs.

• Maintain robust version control documentation trails and content integrity across the lifecycle of scientific materials.

Essential Requirements:

• Education and Experience: Minimum: BSc or equivalent with 8 years relevant experience Preferred: Advanced degree (PhD/Postdoc/MD) with 3-4 years of relevant experience.

• Extensive experience in scientific or medical writing within pharmaceutical biotech or healthcare communications environments.

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

• Strong ability to interpret synthesize and communicate complex scientific and clinical data with accuracy and scientific rigor.

• Experience collaborating in matrixed crossfunctional environments (Medical Affairs Clinical Development and related scientific stakeholders). Proven ability to deliver highquality scientific content under tight timelines while managing multiple parallel projects.

• Familiarity with medical review and approval processes documentation management version control and compliance standards.

• Proficiency with digital content platforms and structured/modular content approaches with strong grounding in scientific governance QC processes and templates.

• Fluent oral and written English; additional languages desirable.

Benefits & Rewards:

Competitive salary Sales incentive bonus Pension scheme Share purchase scheme Health insurance 25 days annual leave Flexible working arrangements subsidized dining facilities Employee recognition scheme learning and development opportunities.

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 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: Desired