This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Senior/Principal Medical Writer based in United Kingdom. Join a specialized medical writing team supporting the development of high-quality regulatory documentation for the global pharmaceutical industry. In this role, you will contribute to clinical development programs across multiple therapeutic areas, partnering with scientific teams and industry stakeholders. You will take ownership of complex regulatory documents while combining scientific expertise, writing excellence, and project coordination skills. This position offers the opportunity to make a meaningful impact on healthcare innovation while working in a collaborative, remote environment. You will have the autonomy to lead projects, share expertise, and grow within a team focused on quality, precision, and scientific communication.