Experteer Overview
As a Clinical Research Associate I at PSI, you will lead onsite monitoring and support study progress across therapeutic indications. You’ll build strong relationships with clinical sites and investigators, ensuring data quality and patient safety. The role combines site management, early study startup involvement, and cross-functional collaboration to meet timelines and standards. This is a hybrid, Barcelona-based opportunity with growth and development within a supportive team. You will help drive compliant, high-quality clinical research that advances patient care.

Compensaciones / Incentivos
• Conduct and report onsite monitoring visits
• Involvement in study startup activities
• CRF review, source data verification, and query resolution
• Site communication and management
• Point of contact for in-house support services and vendors




• Communicate study progress with internal project teams
• Participate in feasibility research

Responsabilidades
• College/University degree in Life Sciences
• 1 year of experience as a Study Coordinator or at least 6 months as a Clinical Research Associate
• English and Spanish proficiency; fluent in Catalan
• MS Office proficiency
• Ability to plan, multitask and work in a dynamic team
• Strong communication, collaboration, and problem-solving skills
• Willingness to travel

Requisitos principales
• Stability, long-term cooperation
• Permanent contract
• Competitive salary and benefit package
• Career development
• Onboarding courses about clinical research industry
• Friendly and supportive colleagues

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