Senior Regulatory Affairs Lead — EU CTR/CTIS Expert
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IQVIA in Madrid seeks an experienced Regulatory Affairs professional to lead EU submissions and lifecycle management for clinical trials. You will act as Regulatory Global Team Leader, guide strategy, and coordinate CTIS activities, ensuring compliance and timely delivery across projects.
The role requires 8+ years in regulatory affairs in pharma/biotech/CRO, strong client advisory skills, and ability to mentor juniors while supporting business development and SOP improvements.
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