ICON is a global healthcare intelligence and clinical research organisation focused on bringing new medicines to patients faster. As an Informed Consent Specialist II, you will lead the development, review, and oversight of informed consent documents for complex, general clinical trials while guiding study teams on strategy and ensuring quality standards across regions.You will work closely with sponsors, ethics committees, and regulatory bodies, oversee translations, and mentor junior staff,#J-18808-Ljbffr
📌 Global Informed Consent Lead (Madrid)
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📍 Madrid
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