Sanofi Hiring Senior Medical Information Writer

Sanofi Hiring Senior Medical Information Writer

3 July, 2022

Sanofi Hiring Senior Medical Information Writer

Job Summary

  • Responsible for research and authoring of scientific response documents under the direction of Global Medical Information (GMI) team in support of global and local Medical information activities.
  • Responsible for execution of activities as required in alignment with GMI colleagues.
  • Achieved through a combination of product knowledge, along with editing, writing, document management proficiency.

Essential Job Duties And Responsibilities

  • Collaborates with GMI teams to execute content plans
  • Conducts literature searches and reviews, extracts/summarizes complex data from scientific literature
  • Generates evidence-based, accurate, current, and fair-balanced summaries of data for the creation/maintenance of scientific response documents for products in designated therapeutic area(s)
  • Adapts global scientific response documents for assigned countries
  • Develops responses to escalated inquiries for assigned countries
  • Develops contributions to US NDA Annual Reports
  • Contributes to US compendia reviews
  • Contributes to peer reviews
  • Demonstrates resolve and urgency to accomplish tasks without direct authority or control. Participate in cross-functional project teams as needed. Ensure that assigned projects are completed on schedule.
  • Develops and maintains Therapeutic Area expertise
  • Reviews the content created by peer writers

Knowledge, Skills & Competencies / Language

  • Therapy Area Exposure: Diabetes, Familial hypercholesterolemia, Cardiovascular disease, Multiple sclerosis, Immunology, Oncology, Market access, Emerging market, Generics, Vaccines, vitamins and supplements, Digestive, Allergies, Parkinson, Haemophilia, Rare diseases, Rare blood diseases
  • Stakeholder management
  • Project management
  • Medical Information Procedures


  • Advanced degree in life sciences/ pharmacy/ similar discipline, or medical degree or doctorate degree (PharmD, Ph. D, Master in science, MBA or equivalent)
  • Excellent English language knowledge, written and communication skills
  • >5 years of experience in regulatory writing for the pharmaceuticals / healthcare industry or equivalent experience in clinical setting
  • At least 2-3 years of direct medical information experience in pharmaceutical company
  • Knowledge about literature evaluation and multilevel response development

Apply HERE

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