EPM is partnered with a leading Medical Communications Agency to support a number of projects as they expand their Regulatory Writing team. They are currently looking for a Regulatory Writer (Senior/Principal level). See summary below: Project Overview Project Type: Regulatory Writing (Submissions) Location: United Kingdom (Fully Remote) Contract Type: Permanent, Full-Time Ideal Start Date: Immediately Language Requirements: English Key Responsibilities Transform complex scientific, clinical, and regulatory data into clear, precise, and audience appropriate documentation. Partner with cross functional teams to develop cohesive, scientifically robust narratives that support regulatory strategy and advance innovative medical science. Ensure all deliverables meet applicable regulatory requirements, industry guidelines, and internal quality standards. Conduct in depth research and maintain up to date knowledge of emerging scientific, clinical, and regulatory developments in relevant therapeutic areas. Develop high quality scientific, educational, and occasionally promotional materials that support the communication and adoption of next generation therapies worldwide. Requirements A minimum of 18 months' experience as a medical writer within a Medical Communications agency or similar scientific writing environment. Demonstrated excellence in scientific writing, with a passion for transforming complex concepts into clear, engaging, and accurate content that meets stakeholder needs. Exceptional attention to detail and proven ability to synthesize and communicate intricate information for diverse audiences. A proactive learner who stays informed about evolving scientific, clinical, and industry trends. Energized by collaborative work and thrives in a fast paced, dynamic, and team oriented environment. If this role is of interest to you, please apply directly to learn more. If not, feel free to share with your network.