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IQVIA is seeking a Regulatory Affairs professional to prepare and review regulatory submissions for clinical trials and marketing authorization. You will work under supervision on small projects, coordinate timelines, and support client requests while collaborating with senior staff.
Required are a Lifescience degree and 2+ years in regulatory affairs, plus fluent English and strong communication skills. The role involves cross-country interactions and some training opportunities in a dynamic,
IQVIA is seeking a Regulatory Affairs professional to prepare and review regulatory submissions for clinical trials and marketing authorization. You will work under supervision on small projects, coordinate timelines, and support client requests while collaborating with senior staff.
Required are a Lifescience degree and 2+ years in regulatory affairs, plus fluent English and strong communication skills. The role involves cross-country interactions and some training opportunities in a dynamic,