PRINCIPAL MEDICAL WRITER

This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Principal Medical Writer based in India.

This is a senior-level opportunity for an experienced medical writing professional to lead the development of high-impact regulatory and scientific documents that support global drug development programs. The role combines scientific expertise, strategic leadership, and cross-functional collaboration to deliver high-quality regulatory submissions and evidence-generation projects across multiple therapeutic areas. You will work closely with clinical, statistical, regulatory, and medical teams while serving as a trusted advisor to clients and key stakeholders. In addition to authoring critical documents, you will contribute to process improvements, training initiatives, and operational excellence within the medical writing function. This position offers significant exposure to global regulatory environments and provides the opportunity to influence both scientific communication strategies and team development. It is ideal for a seasoned professional who thrives in a dynamic, client-focused, and quality-driven environment.