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Expert Scientific Writer

Novartis
Novartis
5+ years
preferred by company
10 Jan. 5, 2026
Job Description
Job Type: Full Time Hybrid Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Expert Scientific Writer – Hyderabad, India (Hybrid)

Job ID: REQ-10068366
Posted: December 16, 2025
Location: Hyderabad, India (Hybrid Work Model)
Employment Type: Full-Time | Regular
Division: Research & Development | Business Unit: Development
Experience Required: 5+ years in medical/scientific writing or clinical research


About the Role

Novartis is seeking an Expert Scientific Writer to develop high-quality, evidence-based scientific content across multiple therapeutic areas. The role involves creating publications, core content elements, slide decks, and presentation materials in alignment with strategic scientific narratives. The candidate will own content from concept to final delivery, ensuring accuracy, clarity, and compliance with scientific and regulatory standards.

This position is based in Hyderabad, India, with a hybrid work setup, combining office collaboration with flexible remote work.


Key Responsibilities

  • Demonstrate deep expertise in assigned therapeutic areas and product portfolios.

  • Research, draft, and edit scientific publications, including primary and review manuscripts, abstracts, posters, and presentation slides.

  • Prepare materials for satellite symposia, advisory boards, and internal/external meetings, including speaker briefings and reports.

  • Ensure scientific accuracy, evidence-based content, proper referencing, and grammatical correctness.

  • Conduct internal scientific reviews to maintain content quality and adherence to strategic objectives.

  • Mentor junior writers and assist in onboarding new team members.

  • Perform quality control (QC) and proofreading of scientific documents to meet stakeholder expectations.

  • Communicate complex medical and scientific concepts clearly and concisely to diverse audiences.


Essential Requirements

  • Minimum 5 years’ experience in medical communications, scientific writing, or clinical research.

  • Educational qualifications:

    • B.Sc. or equivalent with 5+ years of clinical research experience

    • OR M.Sc. / M.Pharm with 10+ years of clinical research experience

  • Strong command of English language with excellent oral and written communication skills.

  • Ability to interact confidently with leadership, peers, and external stakeholders.

Desirable Requirements

  • Thorough knowledge of Good Clinical Practice (GCP).

  • Proven ability to work in a matrix, multicultural environment.

  • Demonstrated presentation, stakeholder management, and diplomacy skills.

  • Customer-oriented mindset with attention to detail and high-quality deliverables.


Why Join Novartis?

Novartis is on a mission to reimagine medicine and improve patient outcomes worldwide. Our associates drive our innovations, and we provide a supportive environment where your contributions make a real impact.

Benefits Include:

  • Comprehensive health and wellness programs

  • Career development and mentorship opportunities

  • Flexible hybrid work model

  • Inclusion in Novartis’ global network and diverse work environment

Commitment to Diversity & Inclusion:
Novartis is dedicated to building inclusive teams and equitable workplaces that reflect the patients and communities we serve.