Regulatory Affairs Specialist
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Worldwide Clinical Trials is seeking a Regulatory Affairs Specialist to support submissions across Belgium, France, and the Netherlands. In this remote role, you will partner with cross-functional teams to ensure timely, compliant regulatory submissions and maintain alignment with local and international requirements.
The ideal candidate holds a bachelor’s degree in a life science and has at least one year of clinical research experience, with strong knowledge of ICH GCP and EU directives, plus