Regulatory Compliance Specialist

1 week ago


kwai tsing district, Hong Kong SAR China IQVIA Argentina Full time
About This Role

This is an exciting opportunity to work in a dynamic environment with a leading global provider of clinical research services. As a Clinical Research Associate, you will have the chance to develop your skills and expertise in study site management, regulatory compliance, and project execution.

Our ideal candidate will have a strong background in scientific disciplines or healthcare, with at least one year of on-site monitoring experience. You will also have excellent knowledge of clinical research regulatory requirements, therapeutic and protocol knowledge, and computer skills including proficiency in Microsoft Office and other tools.



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