01 nov
|
Icon Clinical Research
|
Madrid
01 nov
Icon Clinical Research
Madrid
ICON is seeking an Informed Consent Specialist II in Madrid to lead the development, review, and oversight of informed consent documents for complex, general 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. xghoner
Es esencial asegurarse de que cumple con los requisitos como solicitante para este puesto; por favor, lea atentamente la información a continuación.
The role includes mentoring junior staff and shaping best practices across regions.
📌 Global Informed Consent Lead (Madrid)
🏢 Icon Clinical Research
📍 Madrid