Senior Regulatory Affairs Lead — Lifecycle
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IQVIA in France seeks a Senior Regulatory Affairs Specialist to lead country-level regulatory activities for medicinal products, ensuring compliance and lifecycle management across portfolios. You will collaborate with Medical Affairs, Quality, Commercial and Global Regulatory teams, prepare submissions, review labeling and artwork, and stay ahead of regulatory changes to support timely approvals.
This fixed-term 12-month contract offers the opportunity to contribute to strategic regulatory