Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Senior Medical Information Writer

Sanofi
Sanofi
5+ years
Not Disclosed
10 Jan. 22, 2026
Job Description
Job Type: Full Time 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

Senior Medical Information Writer

Company: Sanofi
Department: Sanofi Business Operations (SBO)
Job Type: Full-Time | Permanent
Location: Hyderabad, India
Experience Required: 5–8+ years
Job Level: Senior


Company Overview

Sanofi is a global healthcare leader dedicated to improving lives through innovative medicines and vaccines. With a diverse portfolio spanning specialty care, chronic diseases, and advanced therapeutics, Sanofi leverages science, digital innovation, and global collaboration to deliver meaningful patient outcomes worldwide.

Sanofi Business Operations (SBO) is Sanofi’s global capability center in India, supporting Medical, HEVA, Commercial, and R&D organizations across regions. SBO plays a critical role in delivering high-quality scientific and medical content that supports evidence-based decision-making globally.


Role Overview

The Senior Medical Information Writer is responsible for developing high-quality, evidence-based scientific response documents to support global and local medical information activities. This role requires strong expertise in literature evaluation, medical writing, regulatory compliance, and cross-functional collaboration, particularly within Global Medical Information (GMI) frameworks.

The position demands independent execution, strategic thinking, and the ability to manage complex medical content across multiple therapeutic areas and geographies.


Key Responsibilities

Medical Information & Scientific Writing

  • Conduct comprehensive literature searches and critical reviews of scientific publications.

  • Extract, analyze, and summarize complex clinical and scientific data.

  • Develop and maintain scientific response documents that are accurate, current, evidence-based, and fair-balanced.

  • Adapt global medical information documents to meet country-specific regulatory and medical requirements.

  • Prepare responses to escalated medical inquiries for assigned markets.

  • Contribute to US NDA Annual Reports and US compendia reviews.

  • Participate in peer review of medical content and provide constructive feedback.

Cross-Functional Collaboration

  • Work closely with Global Medical Information (GMI) teams to execute medical content strategies.

  • Collaborate with stakeholders across Medical Affairs, Pharmacovigilance, and Regulatory functions.

  • Participate in cross-functional project teams to ensure timely delivery of assigned deliverables.

Expertise & Leadership

  • Develop and maintain strong therapeutic area expertise.

  • Review and mentor peer medical information writers to ensure consistency and quality.

  • Support continuous improvement of medical writing processes and content strategies.

Planning, Process & Performance

  • Deliver assigned medical information outputs within agreed timelines and quality standards.

  • Assist in medical writing needs assessments for assigned regions and products.

  • Implement content plans and annual deliverables for supported countries.

  • Coordinate with external vendors, as applicable, to deliver content per defined processes.

  • Incorporate end-user feedback to improve content relevance and effectiveness.


Required Qualifications & Experience

Education

  • Advanced degree in Life Sciences, Pharmacy, Medicine, or related discipline
    (PharmD, PhD, MSc, MD, MBA with healthcare focus, or equivalent)

Experience

  • 5+ years of medical writing experience in the pharmaceutical or healthcare industry, or equivalent clinical experience.

  • 2–3+ years of direct Medical Information experience within a pharmaceutical company.

  • Proven experience in developing scientific response documents and medical information deliverables.

Technical & Professional Skills

  • Strong expertise in literature evaluation, data interpretation, and multilevel response development.

  • Excellent medical writing, editing, and document management skills.

  • Strong understanding of medical information regulations and global compliance standards.

  • Ability to manage multiple projects independently with minimal supervision.

  • Strong stakeholder management, communication, and collaboration skills.

  • Excellent command of written and spoken English.


Why Join Sanofi

  • Work with a globally respected healthcare organization with a strong scientific legacy.

  • Contribute to high-impact medical content supporting patients worldwide.

  • Access continuous learning, career development, and global exposure.

  • Be part of a diverse, inclusive, and innovation-driven work environment.


Equal Opportunity Statement

Sanofi is an equal opportunity employer committed to diversity, equity, and inclusion. All qualified applicants will receive consideration without regard to race, color, religion, gender, age, disability, sexual orientation, gender identity, or any other protected characteristic.