ICON is seeking an Informed Consent Specialist II in Madrid to lead the development, review, and oversight of informed consent documents for complex, integral clinical trials.
You will advise study teams on consent strategy, oversee translations and documentation, and liaise with sponsors and ethics committees to ensure compliant consent wording. The role includes mentoring junior staff and shaping best practices across regions.
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📌 Global informed consent lead (Comunidad de Madrid)
🏢 Icon Clinical Research
📍 Comunidad de Madrid
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