Experteer Overview
In this role you will drive site-facing clinical research activities to ensure data quality and patient safety across therapeutic indications. You will collaborate with clinical sites, investigators and internal teams to meet timelines and standards. You will handle monitoring visits, data verification, and regulatory support, contributing to high-quality study execution. This position offers hands-on responsibility in a supportive CRO environment focused on professional growth and impact.

Compensaciones / Incentivos
• Conduct and report SIV, RMV, COV onsite monitoring visits
• Perform CRF review, source document verification and query resolution
• Manage site communication and vendor coordination
• Serve as a contact for in-house support services and vendors
• Update internal project teams on study progress
• Participate in feasibility research
• Support regulatory team in preparing study submission documents




• Prepare and participate in audits and inspections

Responsabilidades
• A degree in Life Sciences and a Master's degree in Clinical Trials are required
• At least 1 year of independent on-site monitoring experience in Spain
• Experience in Phase II and/or III monitoring visits
• Full working proficiency in English and Spanish
• Proficiency in MS Office applications
• Ability to plan, multitask and work in a dynamic team environment
• Communication, collaboration, and problem-solving skills
• Ability to travel

Requisitos principales
• Stability and long-term cooperation
• Permanent full-time contract
• Competitive salary and benefits
• Career development
• Team collaboration and supportive colleagues
• Onboarding courses about clinical research industry

📌 Clinical Research Associate II (Madrid)
🏢 PSI Software
📍 Madrid