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
Qualifications
- 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