ClinicalEvaluationSpecialist

Our mission is to hasten the transition to universally accessible healthcare. We are authorised by governments to assess and grant market access to medical AIs. Our groundbreaking approach enables the most innovative technology to reach patients safely and quickly. Scarlet is the pre-eminent authority on AI medical devices. We serve customers that matter. Companies building bleeding-edge medical AI systems choose Scarlet. We are proud to count the world’s best resourced and most ambitious companies building medical AI as customers. You will be joining a team with product-market fit, flowing data, and exponentially growing revenue. Come help us bring the next generation of healthcare to the people who need it. ABOUT THIS ROLE: Scarlet’s Devices function is a team of clinicians, AI experts, and software engineers, working together to assess and certify the most innovative and impactful medical device software. We pride ourselves on delivering fast and efficient assessments to enable market access, new device updates and ongoing surveillance of a growing portfolio of medical devices. As we continue to scale our activities and certify more and more medical devices, we need clinical and regulatory expertise to provide support across all stages of the customer journey. You’ll join a team of clinical evaluation experts, conducting swift and accurate device assessments, whilst providing knowledge and expertise to internal functions and external stakeholders. YOUR RESPONSIBILITIES: - Get authorised to assess the clinical evaluation processes of the most innovative medical devices in the world - Collaborate with a multidisciplinary team on technical documentation assessments - Create content to help explain complex regulatory topics to customers and prospects - Screen and action regulatory insights from the latest research, standards and guidance - Support the Sales and Customer Experience function by providing regulatory insights on prospects and customers - Work with our Pr