Regulatory Submissions Lead, Clinical Trials

CTI Clinical Trial and Consulting Services in Madrid is seeking a qualified regulatory professional to assist project teams with clinical study compliance requirements. The ideal candidate will have relevant experience in regulatory submissions and a degree in an allied health field.This role involves preparing and reviewing regulatory documentation,...

IQVIA busca un Responsable Regulatorio Senior para dirigir la estrategia y ejecución regulatoria en Europa, especialmente CTR/CTIS. Trabajarás de forma independiente, liderando equipos y gestionando interacciones con autoridades. Se requiere al menos 8 años en regulatory affairs en pharma/CRO, con experiencia en EU CTR y CTIS y habilidades de gestión de...

Roche is seeking a Regulatory Affairs professional to oversee submission compilation for complex diagnostics products and manage cross‑functional, global regulatory strategies from this Sant Cugat location. You will work with teams across regions to influence timelines and approvals, applying strong regulatory knowledge and stakeholder engagement. The role...

A leading consulting firm is seeking a Global CMC Regulatory Affairs Manager Consultant to support a top pharmaceutical company in Barcelona. This role offers the opportunity to provide regulatory insight, author CMC documents, and coordinate activities for market expansion. The ideal candidate will have at least 5 years of experience in regulatory affairs,...

IQVIA in Madrid is seeking a Decentralized Clinical Trial Study Lead (DCTL) to direct DCT studies from planning to delivery, coordinating with technology, site services, regulatory and IT teams. The role emphasizes strategic oversight, proactive issue resolution and maintaining project profitability.The candidate must have a life sciences degree and at least...

Roche Holding AG recherche un responsable de site clinique spécialisé en IVDR et en démarrage d'études pour concevoir, planifier et coordonner les activités de démarrage, de surveillance et de finalisation des études cliniques sur les sites assignés. Le candidat idéal gérera les soumissions EC/CA, supervisera les prestations CRO et agira en tant...

Warman O'Brien está buscando un Biostatistician Principal para liderar Biostatistics y programming en ensayos clínicos complejos en España. Trabajarás como parte de soluciones FSP para sponsors y colaborarás estrechamente con directores y equipos de liderazgo. Se requiere MS/PhD en estadística/biostatística y experiencia en CRO o entorno...

IQVIA sponsorship- dedicated Clinical Functional Service Partnerships (Clinical FSP) department supports our client’s project team in executing clinical trials. The Clinical Operations Lead coordinates with the trial team, CROs, and vendors to align timelines and deliverables across multiple sites and therapeutic areas. The role requires at least 3 years...

Warman O'Brien en España busca un Biostatistician Principal para liderar Bioestadística y Programación en estudios complejos de FSP integrándose en equipos de patrocinadores y trabajando en proyectos farmacéuticos globales. Se requiere título de M.S. o Ph.D. en estadística o bioestadística y experiencia en CRO o farmacéutica, con capacidad para...