Senior Medical Information Writer

Sanofi; Hyderabad; On-site; INR 1,200,000 - 1,800,000; Full time

Job summary

Sanofi Global Hub in Hyderabad seeks an experienced Senior Medical Information Writer to develop scientific responses and adapt global documents for regional needs.

You will conduct literature reviews, summarize complex data, and create fair-balanced evidence for medical information activities. Collaboration with GMI teams, feasibility in NDA reports, and timely delivery are core expectations.

Qualifications

• 5+ years in medical writing for pharma or healthcare settings.
• 2–3+ years in medical information writing within a pharmaceutical company.
• Excellent editing and medical writing proficiency.
• Understanding regulatory requirements for supported countries is preferred.

Responsibilities

• Conduct literature searches, extract data, and summarize complex data.
• Create evidence-based, fair-balanced scientific summaries for responses.
• Adapt global documents for assigned countries and respond to inquiries.
• Contribute to NDA annual reports and compendia reviews as needed.
• Review content produced by peers and maintain therapeutic area expertise.
• Collaborate with Global Medical Information teams to execute content plans.
• Work with cross-functional teams to ensure on-schedule delivery.

Skills

Stakeholder management

Communication skills

Independent work

Team collaboration

Education

Advanced degree in life sciences/pharmacy/related discipline

Job description

## Senior Medical Information WriterApply: Hyderabad: Full time: Posted Today: End Date: October 31, 2026 (29 days left to apply): R2872299**Our Team:***Sanofi Global Hub is an internal Sanofi resource organization based in India and is set up to centralize processes and activities to support Specialty Care, Vaccines, General Medicines, CHC, CMO, R&D, Data & Digital functions. Sanofi Global Hub strives to be a strategic and functional partner for tactical deliveries to Medical, HEVA, and Commercial organizations in Sanofi, globally.***Main responsibilities:***Responsible for research and authoring of scientific response documents under the direction of the Global Medical Information (GMI) team in support of global and local medical information activities. Responsible for the execution of activities as required in alignment with GMI colleagues. Achieved through a combination of product knowledge, along with editing, writing, and document management proficiency.****Essential Job duties and responsibilities:** 1)* *Conducts literature searches and reviews, and extracts/summarizes complex data from the scientific literature. 2) 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). 3) Adapts global scientific response documents for assigned countries. 4) Develops responses to escalated inquiries for assigned countries. 5) Develops contributions to US NDA Annual Reports. 6) Contributes to US compendia reviews. 7) Contributes to peer reviews. 8) 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. 9) Develops and maintains Therapeutic Area expertise. 10) Reviews the content created by peer writers. 11) Collaborates effectively with Global Medical Information teams to execute content plans** *People: 1) Maintain effective relationships with the end stakeholders (Medical scientific community) within the allocated Global business unit and product – with an end objective to develop medical information content as per requirement. 2) Interact effectively with stakeholders in medical and pharmacovigilance departments. 3) Constantly assist other medical information writers in developing knowledge and sharing expertise.** *Performance: Provide deliverables (scientific response documents, US NDA Annual Reports, US compendia reviews) as per agreed timelines and quality** *Process: 1) Act as an expert in the field of medical information writing and maintain on the regulatory requirement for countries supported. 2) Assist the assigned medical information team in conducting a comprehensive medical writing needs analysis. 3) Implement relevant elements of content plans and associated activities for the year identified for the assigned countries. 4) Work with selected vendors within the region to deliver the required deliverables as per the defined process. 5) Design an overall plan of action basis end-customers feedback & improve course content and delivery.** *Stakeholders: 1) Work closely with medical teams in regions/areas to identify medical writing needs and assist in developing assigned deliverables. 2) Liaise with the Medical department to prepare relevant & customized deliverables.****About you**** **Experience**: *>5 years of experience in medical writing for the pharmaceuticals/ healthcare industry or equivalent experience in a clinical setting; At least 2-3 years of direct medical information experience in a pharmaceutical company** **Soft skills**: *Stakeholder management; communication skills; and ability to work independently and within a team environment** **Technical skills**: *As applicable (Including but not limited to* *Medical operational excellence, time, and risk management skills, Excellent technical (medical) editing and writing skills, Knowledge about literature evaluation and multilevel response development)** **Education**: *Advanced degree in life sciences/ pharmacy/ similar discipline, or medical degree or doctorate degree (PharmD, Ph.D, Master in science, MBA or equivalent)** **Languages**: *Excellent knowledge of the English language (spoken and written)*