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Regulatory Program Management - Sponsor Dedicated

IQVIA

madrid, madrid, Spain Full-time July 15, 2026

Found Description

Experteer Overview
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In this role you will lead regulatory program efforts to align product and regulatory strategies across global filings. You will partner with PMT, GRT, and CDT to translate strategy into executable deliverables, drive cross-functional submission plans, and monitor progress. You will own regulatory project plans and reporting, shaping decisions at PMT, GRT, and CDT levels. You will operate across NA-EMEA-APJLA with Health Authority interactions, ensuring timely and compliant submissions. This is a remote, global role with a focus on high-impact, strategic execution that accelerates development and launch.
Compensaciones / Beneficios
• Provide end-to-end regulatory project management from late development through launch
• Represent Regulatory Program Management at the GRT
• Translate regulatory strategy into actionable delive...

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