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Senior Medical Information Writer

5+ years
Not Disclosed
10 Nov. 13, 2025
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

📍 Location: Hyderabad, India
🏢 Company: Sanofi
🕒 Employment Type: Full-time
🔹 Category: Medical Affairs / Medical Writing


🌍 About Sanofi

Sanofi is a global healthcare leader driven by science and innovation. We are committed to transforming the practice of medicine through breakthroughs in immunology, chronic disease care, and other key therapeutic areas.
Your work here will directly impact millions of patients worldwide—delivering treatments for diabetes, cardiovascular diseases, and transplant complications.

We are harnessing the power of AI, digital transformation, and data-driven research to accelerate progress.
If you’re ready to challenge limits and shape the future of healthcare—this is where ambition meets impact.


🎯 Job Summary

The Senior Medical Information Writer will be responsible for researching, authoring, and maintaining scientific response documents under the guidance of the Global Medical Information (GMI) team. The role focuses on ensuring accuracy, consistency, and compliance with regulatory and scientific standards across global and local medical information activities.


🧩 Key Responsibilities

Scientific Content Development

  • Conduct literature searches and extract complex data from scientific sources.

  • Prepare evidence-based, accurate, and balanced scientific response documents.

  • Adapt global scientific responses for assigned countries.

  • Develop responses to escalated medical inquiries and contribute to US NDA Annual Reports.

  • Support US compendia reviews and peer review activities.

  • Maintain up-to-date knowledge of assigned therapeutic areas.

  • Review and provide feedback on content created by peer writers.

Project & Process Management

  • Plan and execute assigned writing projects within timelines and quality benchmarks.

  • Participate in cross-functional project teams as needed.

  • Ensure deliverables meet compliance, regulatory, and scientific accuracy standards.

  • Support GMI content plans and assist in yearly medical writing needs analysis.

  • Collaborate with vendors and ensure timely project completion.

  • Continuously refine content based on feedback and evolving medical insights.

Stakeholder Collaboration

  • Maintain effective relationships with global and local medical information stakeholders.

  • Collaborate with medical and pharmacovigilance departments to ensure accurate information dissemination.

  • Provide mentorship and share expertise with other medical writers.

  • Work closely with regional medical teams to develop customized scientific deliverables.


👥 Performance Expectations

  • Deliver scientific response documents and related outputs on time and with high quality.

  • Ensure adherence to medical information writing standards, country regulations, and content guidelines.

  • Contribute to continuous process improvement through medical writing excellence and innovation.


🎓 Qualifications

Education

  • Advanced degree in Life Sciences, Pharmacy, Medicine, or related field.

  • Preferred: PharmD, Ph.D., MSc, MBA, or equivalent advanced degree.

Experience

  • Minimum 5+ years of experience in medical writing within the pharmaceutical or healthcare industry.

  • At least 2–3 years of direct experience in Medical Information within a pharmaceutical company.

Technical Skills

  • Strong knowledge of medical information processes and regulatory requirements.

  • Expertise in scientific literature evaluation, response development, and document management.

  • Excellent medical writing and editing skills with attention to detail.

  • Proficiency in time management, project coordination, and risk management.

Soft Skills

  • Strong communication and stakeholder management skills.

  • Ability to work independently and collaboratively within cross-functional teams.

  • Commitment to quality, accuracy, and continuous learning.

Languages

  • Excellent command of English (written and spoken).


💡 Why Join Sanofi

At Sanofi, we believe in:

  • Empowering innovation through science and collaboration.

  • Providing a diverse and inclusive environment where all voices are valued.

  • Investing in your growth, learning, and career development.

  • Driving change to improve people’s lives globally.

Pursue Progress. Discover Extraordinary.
Join us and help create a new era of transformative healthcare.


⚖️ Equal Opportunity Statement

Sanofi is an equal opportunity employer. We value diversity and are committed to creating an inclusive environment for all employees, regardless of race, gender, age, disability, or background.


📽️ Explore More

Watch: “One Day at Sanofi”
Learn more about our Diversity, Equity & Inclusion initiatives at sanofi.com