Amgen in Argentina is seeking a Clinical Trials Regulatory Submission Associate to support regulatory submissions and lifecycle activities under the Local Regulatory Affairs team.
You will collaborate with internal teams to prepare, review, and submit documentation, maintain tracking tools, and ensure compliance with local regulations and GCP. This role requires strong organizational skills and fluent English communication in a general biotech environment.
📌 Regulatory Trials Submission Specialist – Argentina (Buenos Aires)
🏢 Amgen
📍 Buenos Aires
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