This position is listed on behalf of a partner company, which manages all applications and next steps. Our partner is looking for a Principal Medical Writer based in India (Fully Remote). As a Principal Medical Writer, you will lead the development of high-quality clinical and scientific documents that support clinical research and regulatory submissions. You will take ownership of complex writing projects, ensuring that documentation meets scientific, regulatory, and quality standards. Working closely with internal teams and external stakeholders, you will provide strategic guidance on document development, therapeutic area requirements, and industry best practices. You will also review critical deliverables, mentor junior medical writers, and contribute to continuous improvement initiatives. This role offers the opportunity to apply your scientific expertise to meaningful clinical development programs while collaborating with multidisciplinary teams. You may also support program management activities, helping ensure projects are delivered efficiently, on schedule, and in line with client expectations.