Descripción de la oferta
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 writing, with strong literature review and data analysis skills, and be fluent in English.
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