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ICON plc is seeking a Clinical Research Associate II to work remotely in Spain.
Obtenga más información sobre las tareas generales relacionadas con esta oportunidad a continuación, así como sobre las habilidades requeridas.
You will design and analyse clinical trials, interpret complex data, and contribute to innovative therapies.
Responsibilities include monitoring visits, data review, and collaboration with investigators to ensure study success.
Required: 3+ years as a CRA, oncology experience, and strong knowledge of ICH‑GCP.
Travel up to 60% and the ability to work independently in a fast‑paced environment are essential. xqbhyrx