Worldwide Clinical Trials in Barcelona seeks a Clinical Operations Site Management professional to advance data quality and trial integrity across sites. You will collaborate with a diverse, integral team to ensure timely data submission and rigorous regulatory compliance. The role requires strong communication, ability to work remotely as needed, and experience with TMF filing, IRB processes, and site feasibility. Fluency in English and another European language is valued.
📌 In-House Clinical Research Associate | Remote-Ready (España)
🏢 Worldwide Clinical Trials
📍 España
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