Support the development and implementation of the DMHT AI regulatory sandbox
Assist senior colleagues in various compliance activities
Engage with internal and external stakeholders to ensure access to safe medical devices
Collaborate with the safety and surveillance team for compliance activity on digital mental health technologies
Requirements
Proven customer service skills to deal confidently and diplomatically with external stakeholders and colleagues at all levels
Experience of a flexible and adaptable attitude towards work, providing a proactive service and the ability to use initiative, foresight, and have a willingness to go the ‘extra mile’ and excellent attention to detail
Regularly monitor your own and team’s work against milestones ensuring individual needs are considered when setting tasks
Previous experience in software, AI or medical device regulation, including in a clinical, commercial, academic or policy setting. This could include experience developed through previous roles in Regulatory Affairs, Quality Assurance or Medical Affairs
Bachelor’s degree of equivalent in a scientific, engineering or medical discipline
Benefits
Flexible, hybrid way of working
Minimum of 8 days per month working on site
Internal move, temporary promotion, loans will be considered