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

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