Job Title: Senior Medical Information Writer
Company: Sanofi
Location: Hyderabad, India
Company Overview
Sanofi is a global healthcare leader focused on delivering treatments for chronic diseases, immunology, diabetes, cardiovascular disease, and transplant-related complications. The organization leverages advanced technology, AI, and digital tools to accelerate innovation, expand access, and improve patient outcomes worldwide.
Job Summary
The Senior Medical Information Writer will research, author, and maintain scientific response documents in alignment with the Global Medical Information (GMI) team. This role supports both global and local medical information activities, ensuring accurate, evidence-based communication for healthcare professionals and regulatory stakeholders.
Key Responsibilities
Scientific Writing & Content Creation
Conduct literature searches, reviews, and summarize complex scientific data.
Generate evidence-based, accurate, and fair-balanced summaries for scientific response documents in designated therapeutic areas.
Adapt global scientific response documents for assigned countries.
Develop responses to escalated inquiries and contribute to US NDA Annual Reports and US compendia reviews.
Participate in peer reviews and provide feedback on content created by other writers.
Maintain expertise in assigned therapeutic areas.
Collaboration & Stakeholder Management
Maintain effective relationships with medical and pharmacovigilance teams and other key stakeholders.
Collaborate with regional and global medical information teams to execute content plans.
Assist other medical information writers in developing knowledge and sharing expertise.
Performance & Project Management
Deliver scientific response documents, NDA reports, and compendia reviews on schedule and with high quality.
Conduct medical writing needs analysis and implement content plans for assigned countries.
Coordinate with selected vendors to deliver required deliverables per defined processes.
Continuously improve content and delivery based on end-customer feedback.
Process & Compliance
Maintain expertise in medical information and regulatory requirements for supported countries.
Act as an expert in the field to ensure compliance with regulatory and operational standards.
Support cross-functional project teams as needed.
Qualifications
Experience
>5 years in medical writing within pharmaceuticals/healthcare, or equivalent clinical experience.
At least 2–3 years of direct medical information experience in a pharmaceutical company.
Technical Skills
Medical operational excellence, time, and risk management.
Advanced scientific writing and editing skills.
Expertise in literature evaluation and multi-level response development.
Soft Skills
Strong stakeholder management and communication skills.
Ability to work independently and within a team environment.
Languages
Excellent written and spoken English proficiency.
Why Work at Sanofi
Opportunity to break new ground in healthcare innovation and treatment.
Work on a diverse portfolio impacting millions of patients globally.
Grow professionally while leveraging cutting-edge AI and digital tools.
Engage in a culture promoting Diversity, Equity, and Inclusion.
Inclusion & Diversity
Sanofi is an Equal Opportunity Employer. Employment decisions are made without regard to:
Race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, protected veteran status, or other legally protected characteristics.
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