Clinical Evaluation Specialist

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 ResponsibilitiesCollect, review, and interpret clinical data from a range of post-market and clinical follow-up sourcesProduce and maintain Clinical Evaluation Reports and associated documentationManage timelines for ongoing updates across multiple devicesDevelop and refine Clinical Evaluation Plans and safety/performance summariesCollaborate with cross-functional teams to identify evidence gaps and support follow-up strategiesContribute to Post-Market Surveillance and Post-Market Clinical Follow-Up activitiesRequirementsProven experience writing Clinical Evaluation Reports for medical devicesStrong ability to interpret and present clinical data clearly and effectivelySolid understanding of clinical evaluation processes and regulatory expectationsExperience critically reviewing scientific literatureConfident working independently while ..... full job details .....