Are you a detail-driven scientific writer with a passion for turning complex clinical data into clear, compelling evidence? We're partnering with a forward-thinking medical devices company to find a Clinical Evaluation Writer who will play a pivotal role in supporting regulatory success and patient safety across a diverse portfolio on a 6 month contract. As a Clinical Evaluation Writer, you'll take ownership of developing and maintaining key clinical and regulatory documentation. You'll analyse global clinical data, interpret findings, and translate them into robust, compliant reports that support product lifecycle management. Key Responsibilities Collect, review, and interpret clinical data from a range of post-market and clinical follow-up sources Produce and maintain Clinical Evaluation Reports and associated documentation Manage timelines for ongoing updates across multiple devices Develop and refine Clinical Evaluation Plans and safety/performance summaries...