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Senior Scientific Writer I

Novartis
3-5 years
Not Disclosed
Hyderabad
8 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 I

Company: Novartis
Job ID: REQ-10076530
Location: Hyderabad (Hybrid)
Functional Area: Research & Development – Medical Communications
Employment Type: Full-time, Regular
Posted Date: 21 May 2026


Job Summary

This is a senior-level scientific writing role responsible for independently delivering high-quality medical and scientific communication deliverables across multiple therapeutic areas. The role focuses on transforming complex clinical data into clear, compliant, and publication-ready content while managing multiple stakeholders and ensuring adherence to global medical communication standards.

The position also includes mentoring junior writers and contributing to process improvements and publication strategy discussions.


Key Responsibilities

1. Scientific Writing & Content Development

  • Independently develop scientific and medical communication materials, including:

    • Manuscripts (primary and review articles)

    • Abstracts, posters, and oral presentations

    • Slide decks and medical education materials

    • Congress materials

    • Advisory board outputs

    • Internal medical communication documents

  • Interpret and synthesize data from:

    • Clinical Study Reports (CSRs)

    • Statistical Analysis Plans (SAPs)

    • Published literature

  • Ensure all content is:

    • Scientifically accurate

    • Evidence-based

    • Audience appropriate

    • Balanced and compliant


2. Project Ownership & Execution

  • Independently manage multiple complex scientific writing projects.

  • Oversee full project lifecycle:

    • Timeline planning

    • Coordination of reviews (internal, external, QC)

    • Risk identification and escalation

    • Delivery within deadlines

  • Ensure alignment with stakeholders on project milestones and outputs.


3. Stakeholder Management

  • Act as primary scientific writing contact for assigned projects.

  • Collaborate with:

    • Medical Communications Directors

    • Subject matter experts (SMEs)

    • Internal reviewers

    • External authors (where applicable)

  • Lead discussions and manage conflicting feedback effectively.

  • Ensure stakeholder alignment on content direction and quality expectations.


4. Quality, Compliance & Governance

  • Ensure adherence to:

    • Internal SOPs and process guidelines

    • Publication standards such as GPP3

    • Medical communication best practices

  • Perform:

    • Quality control (QC) reviews

    • Data verification

    • Reference checking

  • Maintain audit readiness through accurate documentation and archiving.


5. Coaching & Team Support

  • Provide mentorship and guidance to junior scientific writers.

  • Support:

    • Onboarding of new team members

    • Skill development and training

    • Knowledge sharing initiatives

  • Contribute to continuous improvement of team processes and standards.


6. Strategic & Value Contribution

  • Contribute input into:

    • Publication planning

    • Content sequencing

    • Communication strategy

  • Recommend:

    • Optimal storytelling approaches

    • Format selection for scientific outputs

  • Support process optimization initiatives.


Required Qualifications

Experience

  • 3–5 years of scientific or medical writing experience

  • Preferably in:

    • Pharmaceutical industry

    • Medical communications agencies

  • Demonstrated ability to independently manage complex writing deliverables.


Skills & Competencies

  • Strong scientific writing and data interpretation skills

  • Understanding of:

    • Publication planning

    • Medical communication workflows

    • Clinical data interpretation

  • Strong project management and prioritization skills

  • Ability to work in matrix and global environments

  • Stakeholder communication and negotiation skills

  • High attention to detail and quality orientation

  • Ability to mentor junior writers


Educational Requirements (Preferred)

  • Bachelor’s degree in:

    • Life Sciences

    • Healthcare-related fields

  • Preferred advanced degrees:

    • MSc

    • PhD

    • PharmD

    • MD


Working Conditions

  • Hybrid role based in Hyderabad

  • May require availability during US business hours (up to ~8:00 p.m. IST) for coordination and global collaboration.


Core Responsibilities Summary (Simplified)

This role focuses on:

  • Writing scientific publications and medical content

  • Managing multiple writing projects end-to-end

  • Ensuring compliance and publication quality standards

  • Coordinating with global stakeholders

  • Mentoring junior writers

  • Contributing to publication strategy and process improvement


Core Skill Areas

  • Medical & scientific writing

  • Publication planning

  • Clinical data interpretation

  • Project management

  • Stakeholder engagement

  • Regulatory & publication compliance (GPP3, SOPs)

  • Team mentoring

  • Cross-functional collaboration