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 / Ventajas
- 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