Clinical Affairs Manager — Ai Samd

Legit. Health is seeking a Clinical Affairs Manager to own clinical evaluation and regulatory documentation end-to-end, acting as the expert in the room for European and US submissions. The role requires leading CEP/CER development, post-market follow-up, and regulatory strategy with cross-functional teams. You will design and defend our clinical evidence...

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 seeks a Clinical Affairs Manager to own clinical evaluation and regulatory documentation end-to-end, collaborating with Quality, Regulatory, and Product Development while leading clinical conversations.You will build a network of consultants, design budgets for the clinical evidence department, manage data with traceability, and author SAP and...

Legit.Health is seeking a Clinical Affairs Manager to own our clinical evaluation and regulatory documentation end-to-end with full technical and scientific confidence. You will work closely with Quality, Regulatory and Product Development teams, but you will not depend on them to lead clinical conversations. Find, interact with and coordinate a network of...

Legit.Health is seeking a Clinical Affairs Manager to own our clinical evaluation and regulatory documentation end-to-end with full technical and scientific confidence. You will work closely with Quality, Regulatory and Product Development teams, but you will not depend on them to lead clinical conversations. Find, interact with and coordinate a network of...

About The RoleWhat if your clinical trial expertise could directly shape how AI understands and navigates the complexities of healthcare research? We're looking for experienced Clinical Study Managers to oversee the operational execution of clinical trials — ensuring studies run on time, within budget, and to the highest quality standards — while...

About usSunday, September 20]About usLegit.Health deploys computer vision and artificial intelligence medical devices to enable lifesaving diagnosis and therapies for visible diseases.Our goal is to enable universal access to high-quality diagnosis and follow-up of pathologies and to offer affordable health assistance to everyone everywhere.We are...

OverviewAt Docplanner Group, we’re on a mission to help people live longer, healthier lives. As the world’s largest healthcare platform, we connect millions of patients with doctors across 13 countries. Our marketplaces, SaaS and AI tools simplify daily tasks and help doctors, clinics and hospitals work more efficiently so they can focus on caring for...

Job Overview This role is accountable for performance and compliance for assigned protocols in a country in compliance with ICH/GCP and country regulations, Sponsor policies and procedures, quality standards and adverse event reporting requirements internally and externally.Under the oversight of the Line manager, the person is responsible for budget/finance...