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Senior Scientific Writer Ii

Novartis
2+ years
Not Disclosed
Hyderabad
9 May 26, 2026
Job Description
Job Type: Full Time Hybrid Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Senior Scientific Writer II

Company: Novartis
Job ID: REQ-10077909
Location: Hyderabad (Hybrid)
Functional Area: Research & Development – Medical Communications
Business Unit: Marketing / International
Employment Type: Full-time, Regular
Posted Date: 19 May 2026


Job Summary

The Senior Scientific Writer II role is a high-level scientific communications position responsible for developing and delivering complex, compliant, and strategy-aligned medical content across therapeutic areas.

The role focuses on transforming clinical and scientific data into high-impact communication materials that support global medical affairs strategy, congress activities, advisory boards, and internal/external scientific engagement.

It requires strong therapeutic expertise, advanced scientific writing capability, and the ability to operate effectively in a global matrix environment.


Key Responsibilities

1. Scientific Content Development

  • Develop high-quality medical and scientific materials including:

    • Medical education slide decks

    • Congress and symposia content

    • Advisory board materials

    • Internal scientific communication assets

    • Speaker briefing documents and congress support materials

  • Translate complex clinical/scientific data into:

    • Clear

    • Accurate

    • Evidence-based

    • Strategically aligned narratives

  • Ensure alignment with therapeutic area (TA) strategy and brand scientific narrative.


2. Congress & Medical Communication Support

  • Lead development of congress-related materials such as:

    • Satellite symposia agendas

    • Presentation slides

    • Scientific briefing packages

  • Ensure consistency of messaging across global congress activities.


3. Matrix Collaboration & Stakeholder Engagement

  • Collaborate with cross-functional stakeholders including:

    • International Medical Affairs (IMA / IMACE)

    • Global Medical Affairs (GMA)

    • Clinical teams

    • Medical and commercial stakeholders

  • Participate in discussions to:

    • Align scientific messaging

    • Refine content strategy

    • Ensure accuracy and consistency

  • Work across multiple brands and therapeutic areas simultaneously.


4. Quality, Compliance & Governance

  • Ensure all deliverables comply with:

    • Internal SOPs

    • Regulatory requirements

    • Governance frameworks

    • Medical writing standards

  • Maintain:

    • Version control

    • Documentation integrity

    • Audit-ready content trails

  • Apply structured QC processes and approved templates.


5. Project Management & Delivery

  • Manage multiple concurrent scientific writing projects.

  • Ensure:

    • Timely delivery

    • High-quality output

    • Effective prioritization across workloads

  • Handle complex, fast-paced deliverables under tight deadlines.


Required Qualifications

Education & Experience

  • Minimum:

    • BSc or equivalent + ~8 years relevant experience

  • Preferred:

    • Advanced degree (PhD / MD / Postdoc) + 3–4 years experience


Domain Experience

  • Extensive experience in:

    • Scientific / medical writing

    • Pharmaceutical, biotech, or medical communications environments

  • Minimum 2 years experience in at least one therapeutic area:

    • Oncology

    • Cardiovascular

    • Renal

    • Neuroscience

    • Immunology


Core Skills

  • Strong ability to interpret and synthesize complex clinical/scientific data

  • High-level scientific writing and storytelling skills

  • Experience in matrix/global team environments

  • Strong project management and multitasking capability

  • Familiarity with:

    • Medical review processes

    • Compliance systems

    • Documentation and version control

  • Proficiency in digital content platforms and structured content development


Key Competencies

Scientific & Technical

  • Advanced scientific communication

  • Clinical data interpretation

  • Publication-quality writing

  • Therapeutic area expertise


Collaboration & Stakeholder Management

  • Cross-functional coordination

  • Global stakeholder engagement

  • Consensus-building in matrix environments


Quality & Compliance

  • GPP / internal medical writing standards

  • QC and review processes

  • Regulatory alignment

  • Content governance and audit readiness


Execution & Leadership

  • Managing multiple high-complexity projects

  • Independent ownership of deliverables

  • Ability to influence scientific narrative strategy


Core Role Summary (Simple Version)

This role focuses on:

  • Creating high-level scientific content for global congresses and medical affairs

  • Translating complex clinical data into strategic communication materials

  • Managing multiple global writing projects simultaneously

  • Ensuring compliance, quality, and consistency across scientific messaging

  • Working closely with global medical and clinical teams

  • Supporting therapeutic area communication strategy