PHARMAFull-time
Medical Information Writer
By Admin · Medical Affairs & MSL
HYDERABAD (IN)ONSITEPOSTED: 9/30/2026
PHARMAFull-time
HIRING ORGANIZATIONSANOFIPharmaceuticals / Biotechnology
ROLE OVERVIEW
Medical Information Writer responsible for researching, authoring, adapting, and maintaining evidence-based scientific response documents that support global and local medical information activities across assigned therapeutic areas.
ROLE DEFINITION & RESPONSIBILITIES
- •Conduct literature searches and reviews and extract or summarize complex scientific data
- •Generate accurate, current, evidence-based and fair-balanced scientific response documents
- •Adapt global scientific response documents for assigned countries
- •Develop responses to escalated medical information inquiries
- •Contribute to US NDA Annual Reports and US compendia reviews
- •Execute medical information projects with guidance from experienced team members or managers and deliver assignments on schedule
- •Develop and maintain therapeutic-area expertise and perform peer quality checks when required
- •Collaborate with Global Medical Information teams and medical and pharmacovigilance stakeholders to execute content plans
Reporting Hierarchy: Reports to an experienced Medical Information supervisor/manager within the Global Medical Information organization; collaborates with regional medical teams, pharmacovigilance teams, global medical information colleagues and selected vendors
* Role responsibilities and qualifications synthesized based on industry benchmark standards.
QUALIFICATIONS & REQUIREMENTS
REQUIRED QUALIFICATIONS
- 2-3 years of medical writing experience in the pharmaceutical/healthcare industry or equivalent clinical-setting experience
- 1-2 years of direct medical information experience in a pharmaceutical company
- Advanced degree in life sciences, pharmacy or similar discipline, MSc, MBA or equivalent
- Excellent spoken and written English
- Strong medical editing and writing skills
- Ability to work independently and collaboratively
PREFERRED QUALIFICATIONS
- •Experience with medical information content planning
- •Experience supporting regulatory or pharmacovigilance stakeholders
- •Knowledge of therapeutic-area content development
- •Experience with peer quality checks and cross-functional project teams
REQUIRED VERIFIED SKILLS
Medical information writing
medical writing
scientific literature review
literature evaluation
evidence synthesis
scientific response documents
medical editing
document management
therapeutic area expertise
multilevel response development
stakeholder management
pharmacovigilance collaboration
COMPENSATION & REWARDS
Salary: Competitive / Disclosed upon candidate shortlisting
Benefits: Standard corporate benefits and employee programs; specific benefits are not disclosed in the provided posting.
No salary or bonus information is disclosed in the provided job posting, so no compensation figures are estimated or inferred.
ORGANIZATION CONTEXT & CULTURE
Sanofi is a global healthcare company focused on developing and delivering medicines and vaccines, with business operations in India supporting global and local functions across multiple healthcare areas.
TEAM SIZE: 100,000+ employees
INDUSTRY: Pharmaceuticals / Biotechnology
Culture: The role emphasizes scientific rigor, cross-functional collaboration, stakeholder engagement, continuous knowledge sharing, and delivery of high-quality medical information content within agreed timelines.
EXPECTED CAREER ROADMAP
The position can provide progression from Medical Information Writer into more senior medical information or medical writing roles, with potential expansion into therapeutic-area ownership, content strategy, project leadership, quality oversight, and broader medical affairs responsibilities depending on performance and organizational opportunities.
APPLICATION ADVISORY
Emphasize 2-3 years of relevant medical writing experience and direct medical information exposure; demonstrate strong literature-search and evidence-synthesis capability; highlight experience creating fair-balanced scientific content; showcase medical editing and writing quality; mention collaboration with medical and pharmacovigilance stakeholders; tailor the application to therapeutic-area knowledge and global/local medical information workflows.
RECOMMENDED TRAINING
1/2
READY TO SUBMIT?
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