At Fortrea, we’re on a mission to accelerate life-changing treatments to patients worldwide. To make that happen, we’re looking for an experienced Regulatory Medical Writer to lead the development of participant narratives and guide our narratives writing team. Remote, UK. Full-time. YOUR DAY TO DAY As a key regulatory Medical Writer, you will project lead the full life-cycle of participant narratives development for Phase II-IV clinical trials creating, reviewing, and finalizing safety narratives for clinical study reports. You´ll take ownership from initial planning through final delivery o the sponsor, ensuring quality, consistency and alignment with sponsor. With minimal supervision, during Planning stage, you will: Lead Kick-off strategy meetings, to align global distributed teams, setting goals, milestones, and critical path forward. Conduct communication strategy meetings to consolidate expert contributions into a cohesive participant narrative. Facilitate comment resolution meetings to manage conflicting comments During document development, you will: Maintain alignment with sponsor goals, project status and milestones across all teams. Foster regular communication with functional leads/reviewers to streamline document development (getting inputs timely, consolidating contributions, answering questions.) Once final data is received: Critically interpret raw study data into clear concise language in participant narratives. WHO YOU WILL WORK WITH Expect variety and visibility, You will coordinate functional leads and reviewers including Biostatistics, Programming, and Project Physician teams, as well as Medical Writers across Europe, the Americas, and Asia-Pacific. YOUR EXPERIENCE Advanced degree in life-sciences (PhD or Masters) Minimum 3 years of regulatory medical writing experience, including 1 year as medical writing project lead Extensive experience in writing and leading safety participant narrative development for Clinical Study Reports PERSONAL/TEAM SKILLS This job requires proactivity, teamwork, and excellent communication skills. You´ll be the nexus where multiple teams´ expertise converge, coordinating and collaborating with stakeholders, steering discussions, driving consensus and facilitating decision-making to propel the document development cycle forward. YOUR CAREER, YOUR WAY At Fortrea, we support your growth—whether you’re passionate about scientific writing or aiming for leadership. With access to training, mentorship, and a global network of experts, you’ll have the tools to shape your own path. Ready to make an impact? Join us and help bring life-changing treatments to patients faster. LI-CV1 LI-Remote Learn more about our EEO & Accommodations request here .