Sanofi looking for Medical Writer

Sanofi is a global life sciences company committed to improving access to healthcare and supporting the people we serve throughout the continuum of care. From prevention to treatment, Sanofi transforms scientific innovation into healthcare solutions, in human vaccines, rare diseases, multiple sclerosis, oncology, immunology, infectious diseases, diabetes and cardiovascular solutions and consumer healthcare. More than 110,000 people in over 100 countries at Sanofi are dedicated to making a difference on patients’ daily life, wherever they live and enabling them to enjoy a healthier life.

Post : Medical Writer I

Job Description
Job Summary
We are looking for a Medical Writer I to support the preparation, review, and delivery of clinical and regulatory documents. The ideal candidate will have a strong scientific background, excellent writing skills, and an understanding of clinical research and drug development processes.

Key Responsibilities
• Author, edit, and review clinical and regulatory documents, including: Clinical Study Reports (CSRs), Interim Study Reports, Informed Consent Forms (ICFs), Safety Update Reports, Patient Narratives
• Conduct literature searches and scientific reviews to support document development.
• Analyze and interpret clinical study data to prepare high-quality scientific content.
• Ensure compliance with ICH-GCP guidelines, SOPs, templates, and regulatory requirements.
• Perform quality checks to ensure data accuracy, consistency, and document integrity.
• Collaborate with cross-functional teams including Clinical Operations, Biostatistics, Data Management, Regulatory Affairs, and Medical Affairs.
• Support document review cycles, manage timelines, and address stakeholder feedback.

Candidate Profile
• Bachelor's or Master's degree in Life Sciences, Pharmacy, Biotechnology, Medicine, or related healthcare discipline.
• Experience within a CRO, pharmaceutical, biotechnology, healthcare, or medical communications organization preferred.

Skills
• Strong clinical and scientific writing skills.
• Good understanding of clinical research, drug development, and regulatory guidelines.
• Experience with medical writing, clinical documentation, or medical communications.
• Excellent written and verbal communication skills.
• Strong attention to detail and organizational skills.
• Proficiency in Microsoft Word, Excel, SharePoint, and document management systems.
• Ability to manage multiple projects and work effectively in a collaborative environment.

Additional Information
Qualification : M.Pharm, B.Pharm, M.Sc, B.Sc
Location : India, Remote
Industry Type : Pharma/ Healthcare/ Clinical research
Functional Area : Medical
End Date : 31st August 2026