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Senior Medical Information Writer Hyderabad, India

0-2 years
Not Disclosed
10 Sept. 12, 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

Medical Information Writer

Location: [Insert Location]
Company: Sanofi


About the Role

As a Medical Information Writer, you will be responsible for researching, authoring, and maintaining scientific response documents to support global and local medical information activities. You will collaborate with Global Medical Information (GMI) colleagues, ensuring high-quality, evidence-based, and compliant deliverables. This role requires strong scientific knowledge, writing proficiency, and the ability to work effectively in cross-functional teams.


Key Responsibilities

Scientific Content Development

  • Conduct literature searches and reviews; extract and summarize complex scientific data.

  • Generate accurate, evidence-based, and fair-balanced summaries for scientific response documents across therapeutic areas.

  • Adapt global response documents to meet local country requirements.

  • Develop responses to escalated inquiries in assigned regions.

  • Contribute to:

    • US NDA Annual Reports

    • US Compendia Reviews

    • Peer Reviews

Collaboration & Stakeholder Engagement

  • Build and maintain effective relationships with the medical and scientific community.

  • Partner with medical and pharmacovigilance departments.

  • Collaborate with GMI teams to implement content plans.

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

  • Provide guidance and peer review support to fellow writers.

Expertise & Compliance

  • Develop and maintain therapeutic area expertise.

  • Stay updated on regulatory requirements across supported countries.

  • Support needs analysis for medical writing and align with annual content plans.

  • Ensure all deliverables comply with regulatory and quality standards.

Performance & Process

  • Deliver assigned projects (e.g., response documents, reports, reviews) within agreed timelines and quality standards.

  • Collect feedback from end-users and continuously improve content and delivery.

  • Coordinate with selected vendors to ensure efficient deliverable execution.


What We’re Looking For

  • Strong background in scientific research and medical writing.

  • Ability to analyze, interpret, and summarize complex scientific data.

  • Proficiency in editing, writing, and document management.

  • Strong collaboration skills with cross-functional and global teams.

  • Ability to manage multiple priorities with urgency and accountability.


Why Join Us

At Sanofi, we are entering a new era of science where your growth is as transformative as the work we do. We encourage you to push boundaries, challenge convention, and build smarter solutions that make a real impact. Together, we pursue progress and discover extraordinary possibilities.


Our Commitment to Diversity & Inclusion

Sanofi is an equal opportunity employer. We value diversity and do not discriminate based on race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, veteran status, or any other characteristic protected by law.

🌐 Learn more: sanofi.com
📺 Watch: One Day at Sanofi