Expert Scientific Writer

Novartis

8+ years

preferred by company

Hyderabad India

10 Jan. 19, 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 – Medical Communications & Regulatory Documentation

Location: Hyderabad, India (Hybrid)
Job Type: Full-Time
Experience Required: 8+ years in medical communications / clinical research
Job ID: REQ-10069613
Date Posted: January 13, 2026

Role Overview

Novartis is seeking an Expert Scientific Writer to author, review, and manage high-quality clinical and safety documentation for regulatory submissions, publications, and medical communications. This role requires deep therapeutic expertise and the ability to translate complex scientific concepts into clear, concise, and audience-appropriate content.

The Expert Scientific Writer will support the full content lifecycle—from initial brief to publication or presentation—ensuring first-time-right delivery and compliance with regulatory and internal quality standards. This position is hybrid-based in Hyderabad and offers opportunities to work with global cross-functional teams across research, clinical operations, and medical affairs.

Key Responsibilities

Author, edit, and review high-quality publications and scientific content, including manuscripts, abstracts, posters, slide decks, advisory board reports, and meeting materials.
Ensure content is scientifically accurate, evidence-based, grammatically precise, and aligned with internal quality standards and regulatory guidelines.
Take ownership of content from brief to final deliverable, ensuring first-time-right quality and timely submission.
Conduct internal scientific reviews and perform quality control (QC) checks as required.
Mentor and support junior writers and new team members, providing guidance on writing standards and document quality.
Collaborate with cross-functional teams including clinical operations, regulatory affairs, biostatistics, and medical affairs to produce consistent and accurate content.
Prepare meeting materials for satellite symposia, advisory boards, and internal/external presentations.
Clearly communicate complex scientific and clinical concepts in audience-appropriate language.

Essential Requirements

Minimum 8 years of experience in medical communications, scientific writing, or clinical research documentation.
Educational Qualification:
- B.Sc. or equivalent science degree with 5+ years clinical research experience, or
- M.Sc./M.Pharm with 10+ years clinical research experience
Proven experience in writing and managing clinical and regulatory documents for drugs, biologics, or medical devices.
Excellent written and verbal communication skills, with the ability to interact confidently with leadership, peers, and external stakeholders.
Strong expertise in assigned therapeutic areas and products, with demonstrated ability to produce first-time-right deliverables.

Desirable Qualifications

Thorough knowledge of Good Clinical Practice (GCP) and regulatory submission standards.
Experience working in matrix and multicultural environments.
Strong presentation, diplomacy, and stakeholder management skills.
Customer-focused mindset with ability to communicate complex scientific information effectively.

Why Join Novartis

Be part of a global leader in medicine, helping to improve and extend lives.
Work in a hybrid, inclusive, and collaborative environment that values diversity and innovation.
Engage with global scientific teams and contribute to cutting-edge publications and regulatory submissions.
Access comprehensive benefits, professional development programs, and wellness initiatives.
Contribute to scientific excellence and patient impact at a world-renowned biopharmaceutical company.

Learn more about Novartis culture, benefits, and career opportunities:
Novartis Careers – Benefits & Rewards

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Expert Scientific Writer India, Medical Writing Jobs Hyderabad, Clinical Writing Jobs India, Regulatory Medical Writer India, Novartis Careers India, Medical Communications Jobs

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Expert Scientific Writer

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