SaMD UX Lead

¿Estás preparado/a para un cambio y explotar tus habilidades como nunca? Sigue leyendo porque tenemos lo que buscas… Somos unaempresa internacionalcon más de 16 años de experiencia en consultoría e ingeniería informática. Con más de2.500 Primersoperando en4 sectoresprincipales en todo el mundo: IT, Telecomunicaciones, Energía e...

Legit.Health is seeking a Clinical Affairs Manager to own end-to-end clinical evaluation and regulatory documentation for EU and US markets. You will lead CEP/CER generation, PMCF programs, and post-market clinical follow-up with strong scientific rigor. You will work independently, shaping the clinical evidence strategy while collaborating with Quality,...

Legit.Health busca un/a Clinical Affairs Manager para hacerse cargo de la evaluación clínica y la documentación regulatoria de extremo a extremo con confianza técnica y científica. Liderarás la estrategia de evidencia clínica para mercados EU y US, trabajando de forma independiente y sin depender de otras áreas para conversaciones clínicas. Serás...

Legit.Health está buscando un/a Gerente de Asuntos Clínicos para liderar la evaluación clínica y la documentación regulatoria end‑to‑end, con confianza técnica y científica. Serás la pieza experta, diseñando y defendiendo la estrategia de evidencia clínica para mercados europeos y FDA. Trabajarás estrechamente con Calidad, Regulación y...

Legit. Health busca un Responsable de Asuntos Clínicos para gestionar la evaluación clínica y la documentación regulatoria de extremo a extremo, con total criterio técnico y científico. Serás la voz experta en evidencias clínicas para presentaciones en EU y FDA. Trabajarás de forma autónoma con Calidad, Regulación y Desarrollo de Producto,...

A leading healthcare platform in Barcelona seeks a Senior Healthcare Regulatory Specialist to ensure compliance with EU Medical Device Regulation (MDR) while driving global expansion. The role involves collaborating across teams to develop a robust regulatory framework, facilitating market access for innovative healthtech products. Ideal candidates have...

Legit.Health is seeking a Clinical Affairs Manager to own clinical evaluation and regulatory documentation end-to-end, working remotely with global teams. You will interact with consultants to gather insights and design SAPs/SARs, ensuring regulatory readiness for SaMD products. You should have 5+ years in clinical trials, regulatory affairs, or medical...

Legit. Health is seeking a Clinical Affairs Manager to own the clinical evaluation and regulatory documentation end-to-end. You will design and defend our evidence strategy, lead CER/CEP creation, and drive PMCF plans for EU and FDA submissions. You will work with Quality, Regulatory, and Product teams but independently lead clinical conversations and...

ResponsibilitiesSet the UX direction for ELL, translating product strategy into design strategy and clear team-level execution priorities.Drive customer experience outcomes across multiple squads, journeys, and surfaces so that learners and teachers experience ELL as one connected system.Own product-area UX quality, consistency, and cohesion; raise UX...