Position: Senior Medical Information Writer
Location: Hyderabad, India
Job Type: Full-time
Sanofi is a global healthcare company focused on delivering innovative treatments across diabetes, cardiovascular disease, transplant care, and other therapeutic areas. The company emphasizes AI and digital tools to accelerate healthcare innovation and expand patient access.
The Senior Medical Information Writer is responsible for researching, authoring, and reviewing scientific response documents under the direction of the Global Medical Information (GMI) team, supporting both global and local medical information activities. The role requires strong writing, editing, and document management skills, combined with therapeutic area expertise.
Content Creation & Medical Writing
Conduct literature searches, reviews, and extract/summarize complex scientific data.
Generate evidence-based, accurate, fair-balanced scientific response documents for assigned therapeutic areas.
Adapt global scientific response documents for assigned countries.
Develop responses to escalated medical inquiries.
Contribute to US NDA Annual Reports and US compendia reviews.
Participate in peer reviews and maintain therapeutic area expertise.
Ensure timely completion of assigned projects and deliverables.
Work on groundbreaking science impacting patients globally.
Leverage AI and digital tools to enhance medical information and healthcare access.
Inclusive and diverse workplace fostering growth and innovation.
Equal opportunities for all employees regardless of protected characteristics.
Soft Skills
Excellent stakeholder management and communication skills.
Ability to work independently and collaboratively within a team.
Strong command of English (spoken and written).
Technical Skills
Medical operational excellence, time and risk management.
Literature evaluation and multi-level response development.
Strong technical editing and writing skills.
Education
Advanced degree in life sciences, pharmacy, medicine, or related field (PharmD, Ph.D., M.Sc., MBA, or equivalent).
Experience
5 years in medical writing in the pharmaceutical or healthcare industry.
2–3 years of direct medical information experience in a pharmaceutical company.
Maintain compliance with regulatory requirements and internal processes.
Performance Metrics
Deliver high-quality scientific response documents, NDA reports, and compendia reviews on time.
Process & Compliance
Act as a subject matter expert in medical information writing and regulatory requirements.
Assist in medical writing needs analysis for assigned countries.
Implement content plans and associated activities as per annual strategy.
Work with vendors to ensure high-quality deliverables.
Continuously improve content based on end-customer feedback.
Stakeholder Management
Maintain effective relationships with Medical and Pharmacovigilance teams, end stakeholders, and other internal teams.
Collaborate with Global Medical Information teams to execute content plans.
Support and mentor other medical information writers by sharing expertise.
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