Experteer Overview
In this role you will drive high-quality clinical research across various indications, maintaining strong site relationships and ensuring data integrity and patient safety. You will support project timelines and regulatory readiness while collaborating with cross-functional teams. The position blends on-site monitoring with feasibility insights and audits, offering meaningful impact on study success. Join PSI to contribute to reliable, timely clinical services within a supportive, development-focused environment.

Compensaciones / Incentivos
• Conduct and report on-site monitoring visits (SIV, RMV, COV) to ensure data quality and protocol compliance
• Perform CRF review, source data verification, and query resolution
• Manage site communications and relationships with investigators
• Serve as a contact for in-house support services and external vendors
• Coordinate with internal project teams on study progress




• Participate in feasibility research
• Support regulatory team with study submission documents
• Prepare for and participate in audits and inspections

Responsabilidades
• Bachelor in Life Sciences
• Master in Clinical Trials
• At least 1 year of independent on-site monitoring experience in Spain
• Experience in Phase II and/or III monitoring visits
• Fluent in English and Spanish
• Proficient in MS Office
• Strong planning, multitasking and teamwork abilities
• Excellent communication, collaboration and problem-solving skills
• Willingness to travel

Requisitos principales
• stability
• permanent contract
• competitive salary
• career development
• team collaboration
• onboarding courses

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