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Senior Scientific Writer I

3-5 years
Not Disclosed
10 Nov. 24, 2025
Job Description
Job Type: Full Time 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

Senior Scientific Writer I – Hyderabad (Hybrid)

Company: Novartis Healthcare Pvt. Ltd.
Location: Hyderabad, India (Hybrid)
Job Type: Full-Time | Regular
Functional Area: Research & Development

Job Overview

Novartis is seeking a highly skilled Senior Scientific Writer I to support the development of high-quality scientific and medical communication materials. This role involves working closely with cross-functional and global teams to create publications, literature reviews, abstracts, posters, slide decks, and manuscripts aligned with regulatory, clinical, and internal medical requirements.

This position is ideal for candidates with proven scientific writing expertise and a strong understanding of clinical research documentation standards.


Key Responsibilities

  • Develop comprehensive literature reviews, abstracts, posters, and slide sets using data from clinical study reports, patient profiles, and related sources.

  • Prepare scientific publications and communication materials that meet regulatory, clinical trial transparency, and brand communication requirements.

  • Perform quality control (QC), proofreading, and document review to ensure accuracy, clarity, and compliance with internal standards.

  • Manage multiple scientific writing projects simultaneously, ensuring timelines and deliverables are met.

  • Collaborate with internal stakeholders and maintain consistent communication to gather feedback and optimize deliverables.

  • Adhere to Novartis editorial guidelines, including Novstyle and approved templates.

  • Track clinical trial milestones for assigned writing projects and maintain comprehensive project documentation and archives.

  • Ensure SOP, audit, and training compliance across all assigned tasks.

  • Support additional scientific writing and documentation tasks as required.


Education Requirements

  • Required: Degree in a healthcare or life science–related field.

  • Preferred: Advanced degree such as PhD, PharmD, or MD in life sciences or healthcare.


Experience Required

  • 3–5 years of professional experience in scientific writing, preferably within the pharmaceutical or clinical research industry.

  • Demonstrated ability to work effectively in matrixed, cross-functional, and multicultural teams.

  • Strong customer-focused approach and proven collaboration skills.


Why Join Novartis?

Novartis is driven by a global mission to reimagine medicine and enhance patients’ lives. By joining our team, you will contribute to impactful scientific communication that supports innovative therapies worldwide.

What You Can Expect

  • Competitive compensation and comprehensive benefits.

  • Access to the Novartis Life Handbook for complete information on benefits and professional development.

  • A culture built on diversity, inclusion, and scientific excellence.

  • Opportunities to grow within a global organization committed to meaningful healthcare advancements.


Diversity, Inclusion & Accessibility

Novartis is committed to creating a workplace that reflects the communities we serve. We provide reasonable accommodations for individuals with disabilities throughout the recruitment process and employment lifecycle.

If you need accommodation, contact: diversityandincl.india@novartis.com (Include Job Requisition ID: REQ-10067340)

 


About Novartis Network

If this role does not fully match your career goals, you may join the Novartis Talent Network to stay informed about future opportunities.