Summary
Operating within an International, matrix environment, the Senior Scientific Writer II partners closely with other Scientific Writers and collaborates cross-functionally with colleagues across IMA (IMACE, TAs), Global Medical Affairs (GMA), and additional clinical, and commercial stakeholders. Through these partnerships, the role drives content excellence, governance, and harmonization across therapeutic areas and markets, contributing to a cohesive and impactful scientific communication strategy.
About the Role
Senior Scientific Writers II
Location – Hyderabad #LI Hybrid
Major 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 congress‑related materials such as satellite symposia agendas, speaker briefing documents, and slide content.
- Research, interpret, and synthesize complex scientific and clinical data into accurate, well‑referenced, evidence‑based content aligned with TA strategies.
- Ensure scientific precision, clarity, and IMACE‑level 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 audit‑ready 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, cross‑functional environments (Medical Affairs, Clinical Development, and related scientific stakeholders). Proven ability to deliver high‑quality 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.
Why Novartis: Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here: https://www.novartis.com/about/strategy/people-and-culture
You’ll receive: You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook. 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.
Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network.
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
Benefits and Rewards: Learn about all the ways we’ll help you thrive personally and professionally.
Read our handbook (PDF 30 MB)
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Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.
Accessibility and accommodation
Novartis is committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to perform the essential functions of a position, please send an e-mail to [email protected] and let us know the nature of your request and your contact information. Please include the job requisition number in your message.
