Principal Scientific Writer

10-12 years

Not Disclosed

India

10 Nov. 27, 2025

Job Description

Job Type: Full Time Hybrid Education: B.Sc/M.Sc/M.Pharma/B.Pharma/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

Principal Scientific Writer – Hyderabad, India

Job ID: REQ-10067341
Location: Hyderabad, Telangana, India
Employment Type: Full-Time, Regular
Work Pattern: Hybrid
Experience Required: 10–12+ years (depending on degree)
Division: US Business Unit – Marketing / R&D

Company Overview

Novartis Healthcare Private Limited is a global leader in reimagining medicine to improve and extend lives. Through innovative science, advanced clinical research, and a patient-focused approach, Novartis develops therapies that make a meaningful impact on healthcare worldwide. Join Novartis to be part of a community of passionate, collaborative professionals shaping the future of medicine. Learn more at novartis.com.

Position Summary

The Principal Scientific Writer will lead, manage, and provide consultancy to senior and expert writers in preparing high-quality medical and scientific communications. This includes literature reviews, abstracts, posters, slide decks, and complex manuscripts intended for publication and professional presentations. The role demands expertise in clinical research, strong scientific writing, and the ability to oversee multiple projects across therapeutic areas while maintaining the highest standards of quality, compliance, and timeliness.

Key Responsibilities

Prepare, review, and support the creation of highly complex scientific documents adhering to regulatory and journal standards (e.g., CONSORT).
Manage multiple projects across brands and therapeutic areas, ensuring timely delivery and quality compliance.
Develop Centers of Excellence (CoE) for specific therapeutic areas, disease states, or deliverables.
Provide strategic input to brand development plans, serving as a TA/disease/deliverable champion.
Implement stakeholder management strategies for internal and external collaborators.
Champion process improvement initiatives, streamline workflows, and enhance team efficiency.
Train and mentor new joiners and colleagues in scientific writing standards and practices.
Maintain project documentation, SOP compliance, and audit readiness.
Contribute actively to knowledge creation, scientific publications, and dissemination activities.

Required Qualifications

Education: Minimum B.Sc. (Science) with 12 years of Clinical Research experience, or M.Sc./M.Pharm with 10 years of Clinical Research experience.
Preferred: PhD (>8 years CR experience), MBBS/MD/equivalent (MD >6 years, MBBS/PhD >8 years CR experience).
Proven expertise in medical writing, scientific documentation, and clinical trial reporting.
Strong analytical, organizational, and project management skills.
Excellent command of English (written and verbal) and proficiency in scientific communication.

Key Performance Indicators (KPIs)

Delivery of high-quality medical and scientific documents for journals, clinical teams, and Health Authorities.
Compliance with journal formatting standards and regulatory guidance (e.g., CONSORT).
Efficient management of projects and teams, ensuring optimal output and quality.
Positive feedback and acceptance of publications by internal and external stakeholders.
Active contribution to knowledge sharing, publications, and scientific communications.

Why Join Novartis

Be part of a global mission to transform patients’ lives through science.
Access to career development, professional growth, and world-class benefits.
Engage in an inclusive and diverse work environment where every voice is valued.
Learn more about Novartis culture, benefits, and rewards: Novartis Life Handbook.

Accessibility & Inclusion

Novartis is committed to providing reasonable accommodations for individuals with disabilities throughout the recruitment process and within the workplace. Applicants requiring accommodations may contact diversityandincl.india@novartis.com with their request and job requisition number.

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Principal Scientific Writer

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