EU Clinical Trials Regulatory Start-Up Lead

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,...

Indero is seeking a Start-Up Manager to oversee multi-country site activation across Europe with a strong focus on timely delivery, regulatory compliance, and cross-functional collaboration. The role emphasizes strategic planning, risk management, and close interaction with sponsors and internal teams. Ideal candidates will have a track record of leading...

CTI Clinical Trial and Consulting Services seeks a regulatory specialist to advise project teams on country-specific regulatory requirements for clinical studies. You will perform compliance assessments, adapt study documents for each country and site, and submit to IRB/EC/CA as needed. The role requires 3–5 years of pharmaceutical regulatory experience,...

CTI Clinical Trial and Consulting Services is seeking an experienced Regulatory Affairs professional to support Study Start-Up (RASSU) activities across multiple countries. You will advise project teams on regulatory requirements and oversee submissions to IRBs/ECs, ensuring quality and compliance across sites. Responsibilities include adapting study...

Grupo Gigas busca un Coordinador de Presentaciones Regulatorias para unirse a su equipo de Operaciones Clínicas en España. Coordinará actividades de inicio de estudio y cumplimiento en entornos multicountry, gestionando documentos regulatorios y acuerdos, y asegurando plazos y calidad.Se valora experiencia en regulación clínica, conocimiento de ICH-GCP...

ICON plc, a world-leading healthcare intelligence and clinical research organization, is seeking a Study Start Up Associate II to drive site activation in Spain from a home-based role. You will coordinate SSU activities, ensure regulatory compliance, and collaborate with internal teams to maintain timelines and quality across trials. You will review...

Fortrea is seeking a Site Start-Up Specialist in Madrid, Spain, to coordinate site activation, manage essential regulatory documents, and ensure timely submissions in line with ICH/GCP guidelines. You will work within the FSPx team, collaborating with sponsors and clinical teams to advance trials.The role requires a life sciences-related degree or allied...

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...

Serms CRO busca un/a Senior en Study Start-Up & Regulatory para liderar procesos regulatorios en ensayos clínicos nacionales e internacionales. Se valorará autonomía y experiencia en gestión de documentación y cumplimiento normativo, con fuerte foco en ICH-GCP y normativa UE.Formarás parte del equipo de Regulación Clínica, reportando a la dirección...