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 coordinate with consultants. Strong GCP, MDR/FDA experience, and English proficiency are essential.#J-18808-Ljbffr
📌 Remote Clinical Affairs Lead For Medtech Samd (Ourense)
🏢 Legit.Health
📍 Ourense
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