Regulatory & Clinical Affairs Pro — Pharma/Devices

A global consulting firm is seeking a Regulatory Affairs / Clinical Affairs Specialist with 5-15 years of experience in pharmaceuticals and medical devices. The role involves managing regulatory projects, advising clients on compliance, and preparing regulatory submissions. Candidates should have a relevant academic background and strong analytical skills. This position offers opportunities for professional development and part-time remote work, as well as a competitive salary. Fluent English is required, and French is a plus.

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