Senior Regulatory Affairs Lead — Eu Ctr/Ctis Expert

Hace 16 horas

madrid, kingdom of spain Affinis Selección De Personal E Headhunting Jornada completa
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. xhfqzwm
Antes de solicitar este puesto, por favor, lea la siguiente información sobre esta oportunidad que encontrará a continuación.
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.