Parexel is seeking a Site Activation Partner to lead or support operational activities from start-up to close-out for assigned studies and sites, ensuring timelines and compliance with GCP and sponsor standards. The role involves initiating IIP, regulatory collaboration, and issue resolution.The position requires 2+ years in clinical trials and site activation, knowledge of ICH/GCP and FDA regulations, and fluency in English and local language.#J-18808-Ljbffr
📌 Site Activation Specialist – Remote Clinical Trials (Santiago de Compostela)
🏢 Parexel
📍 Santiago de Compostela
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