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Senior Medical Information Writer

Sanofi
Sanofi
5-8 years
upto 12 LPA
Hyderabad
10 April 23, 2026
Job Description
Job Type: Full Time Education: B.Pharm, M.Pharm, Pharm D., BSc., MSc. 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

Senior Medical Information Writer – Medical Affairs

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