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A general biopharmaceutical company is seeking a motivated candidate for an entry-level role focused on regulatory document management and support in clinical trials. Responsibilities include assisting with submissions to regulatory authorities, ensuring compliance with guidelines, and serving as the primary contact for investigative sites. Ideal candidates are recent graduates or have relevant experience in life sciences, with a strong desire to learn and grow in a dynamic environment.
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Postúlate en Kit Empleo: kitempleo.cl/empleo/1cz1rn
📌 Clinical Submissions Start-Up Associate (Santiago)
🏢 Fortrea
📍 Santiago
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