Legit.Health is hiring a Clinical Affairs Manager to own clinical evaluation and regulatory documentation end-to-end, with leadership in EC/US submissions. You will craft CEP/CER, oversee PMCF, and build the evidence base while guiding regulatory conversations with QA/Regulatory and Product teams.
You will design and defend evidence strategies for MDR and FDA, translate findings to product teams, and manage multi-geography dossiers with autonomy and scientific rigor.