Regulatory & Submissions Lead — Paris (Hybrid)
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Parexel in France is seeking a Regulatory & Submissions Lead to join our team in a hybrid capacity, with at least two days per week onsite in Paris. The role is accountable for performance and compliance across assigned clinical trial protocols, ensuring adherence to ICH/GCP guidelines and local regulations.
As a key contributor to study startup and execution, you will drive regulatory and ethics submissions, maintain compliance, and support critical milestones through collaboration with cross
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Parexel
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