Senior Scientific Writer II job opportunity at Novartis.

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DatePosted 3 Days Ago bot
Novartis Senior Scientific Writer II
Experience: 8-years
Pattern: full-time
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degreeAssociate
loacation Hyderabad (Office), India
loacation Hyderabad (Off..........India

Job Description Summary The Senior Scientific Writer II develops high quality, accurate, and compliant medical and scientific communications aligned with therapeutic area strategy and the brand’s overarching scientific narrative. The role leads the planning, and delivery of a broad range of scientific materials, including medical education slide decks, medical congress including symposia, advisory board materials, and scientific content supporting congress activities and internal medical engagements. 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. 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.   Job Description 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.   Skills Desired Building Construction, Clinical Practices, Clinical Research, Clinical Trials, Drug Development, Hazard Identification, Health Sciences, Immunology, Intensive Care UnIT (Icu), Internal Control, Internal Medicine, Job Description, Medical Information, Organization Skills, Patient Care, Stakeholder Engagement, Tcp/Ip Protocols, Utilization Management (Um)

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