Experteer Overview As a Global Regulatory Scientist you will shape regulatory strategy for global clinical trials and coordinate submissions in line with ICH-GCP and ICON policies. You’ll work with cross-functional teams to prepare core documentation and drive regulatory plans across jurisdictions. Your role includes coordinating submissions with agencies and ethics committees, tracking progress, and participating in audits and CAPA processes. This is an opportunity to influence global development programs within a values‑driven, inclusive environment that prioritizes well-being and innovation. You will contribute to ICON’s mission to advance clinical development at scale, using your regulatory expertise to deCompensaciones / Incentivos
- Develop and implement global clinical trial submission strategies and regulatory plans with stakeholders
- Prepare, review, and finalize core regulatory documentation to ensure compliance




- Coordinate submissions to regulatory agencies, ethics committees, and country authorities
- Track and report submission progress in ICON systems with accurate documentation
- Represent Regulatory during audits, CAPAs, and client meetings with strategic inputResponsabilidades
- Bachelor’s degree and 0-3 years of regulatory submission experience
- Strong understanding of ICH-GCP and global regulatory guidelines
- Excellent organizational and communication skills with attention to detail
- Willingness to travel approximately 10%Requisitos principales
- annual leave entitlements
- health insurance offerings
- retirement planning
- Global Employee Assistance Programme (LifeWorks)
- life assurance
- flexible country-specific optional benefits

📌 Global Regulatory Scientist (Madrid)
🏢 Icon Clinical
📍 Madrid