Senior Regulatory Affairs Lead — EU CTR/CTIS Expert

Bp is seeking a MED Regulatory Affairs professional to lead Spain regulatory coverage for Supply, Trading & Shipping. You will interpret regulatory developments under RED, ReFuelEU Aviation, and other rules, advising on commercial and compliance implications across Spain.Based in Madrid with a hybrid office/remote setup, you will coordinate with EU teams and...

IQVIA seeks an experienced Regulatory Affairs professional to lead EU CTR/CTIS submissions and lifecycle activities. You will guide strategy, manage regulatory documentation, and liaise with authorities while mentoring juniors and supporting business development.Ideal candidates have 8+ years in regulatory affairs within pharma/biotech/CRO sectors, with...

IQVIA is seeking an experienced Regulatory Affairs professional in Madrid, Spain to lead and manage EU CTR submissions and CTIS lifecycle activities. You will provide strategic regulatory guidance, interact with regulatory authorities, and mentor junior staff while ensuring timely, compliant deliverables. The role requires 8+ years in regulatory affairs...

Job Overview¿Quiere enviar su solicitud? Lea toda la información sobre este puesto a continuación y luego pulse el botón de solicitar.Individual contributor with advanced knowledge acquired from at least 8 years of relevant industry experience. Working independently with limited supervision, the individual will provide strategic regulatory expertise and...

Job Overview ¿Quiere enviar su solicitud? Lea toda la información sobre este puesto a continuación y luego pulse el botón de solicitar. Individual contributor with advanced knowledge acquired from at least 8 years of relevant industry experience. Working independently with limited supervision, the individual will provide strategic regulatory expertise...

LocationsMadrid, SpainBelgrade, SerbiaLisbon, PortugalBudapest, HungaryAthens, GreeceBarcelona, SpainSofia, BulgariaBucuresti, RomaniaContract TypeFull timeJob OverviewIndividual contributor with advanced knowledge acquired from at least 8 years of relevant industry experience. Working independently with limited supervision, the individual will provide...

IQVIA is seeking an experienced Regulatory Affairs professional in Madrid, Spain to lead and manage EU CTR submissions and CTIS lifecycle activities. You will provide strategic regulatory guidance, interact with regulatory authorities, and mentor junior staff while ensuring timely, compliant deliverables. The role requires 8+ years in regulatory affairs...

Job Overview Individual contributor with advanced knowledge acquired from at least 8 years of relevant industry experience. Working independently with limited supervision, the individual will provide strategic regulatory expertise and leadership for clinical trial applications and lifecycle management activities, with a strong focus on EU Clinical Trials...

** Please submit your application in English ** What You'll Do: The Global RASSU Lead will serve as a subject matter expert for clinical trial regulatory requirements, ensuring alignment with country-specific requirements, CTI and sponsor SOPs, ICH/GCP, and applicable regulations. The role will also support regulatory document oversight, study start-up...