Location: Hyderabad, India
Company: Sanofi
Job Type: Full-Time
Experience Required: 5–8 years (Not suitable for freshers)
About the Company
Sanofi is a global healthcare leader focused on advancing scientific innovation to improve lives. With a strong presence across specialty care, vaccines, general medicines, and consumer healthcare, the organization is at the forefront of delivering transformative therapies in areas such as immunology, diabetes, cardiovascular diseases, and transplant care.
Sanofi Business Operations in India acts as a strategic global hub, supporting medical, HEOR, pharmacovigilance, commercial, and digital functions worldwide.
Role Overview
The Senior Medical Information Writer is responsible for developing high-quality, evidence-based scientific content to support global and regional medical information activities. This role requires strong expertise in literature evaluation, scientific writing, and stakeholder collaboration to ensure accurate and compliant communication across therapeutic areas.
Key Responsibilities
Scientific Writing and Content Development
Conduct comprehensive literature searches and critically analyze scientific data
Develop and maintain scientifically accurate, balanced, and up-to-date medical response documents
Adapt global medical content for regional and country-specific requirements
Create responses for complex and escalated medical inquiries
Contribute to regulatory documents including US NDA Annual Reports and compendia reviews
Medical Review and Quality Assurance
Perform peer review of scientific content to ensure quality and compliance
Maintain therapeutic area expertise and ensure scientific accuracy in all deliverables
Ensure adherence to global regulatory standards and internal SOPs
Stakeholder Collaboration
Work closely with global medical information teams, pharmacovigilance, and medical affairs stakeholders
Support cross-functional teams in executing medical content strategies
Engage with internal and external stakeholders to understand medical communication needs
Project and Process Management
Deliver projects within defined timelines and quality benchmarks
Support medical writing needs analysis and execution of annual content plans
Collaborate with regional vendors and internal teams to ensure seamless execution
Continuously improve processes based on stakeholder feedback and evolving business needs
Required Qualifications
Advanced degree in Life Sciences, Pharmacy, Medicine, or related field
5–8 years of experience in medical writing within the pharmaceutical or healthcare industry
Minimum 2–3 years of direct experience in Medical Information (MI) within a pharmaceutical company
Strong expertise in scientific literature evaluation and medical content development
Excellent written and verbal communication skills in English
Proven ability to manage stakeholders and work in cross-functional global teams
Core Competencies
Scientific and medical writing excellence
Regulatory and compliance knowledge
Stakeholder and project management
Analytical thinking and attention to detail
Ability to work independently in a fast-paced global environment
Why Join This Role
Work on global medical communication strategies impacting patient care worldwide
Exposure to cutting-edge therapeutic areas and scientific advancements
Opportunity to collaborate with international teams across medical, safety, and commercial functions
Career growth within a globally recognized pharmaceutical organization
Important Note for Applicants
This is a senior-level role requiring prior experience in medical information and scientific writing. Freshers or entry-level candidates are advised to apply for roles such as Medical Writer Trainee, Drug Safety Associate, or Clinical Research Coordinator to build foundational experience.
How to Apply
Interested candidates can apply through the official careers portal of Sanofi or explore verified global opportunities on ThePharmaDaily.com
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Europe | France | Latvia | Lendava | Leuven | Poland | Slovenia | Spain |Finland :
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Kyiv |Lima Region :
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