Experteer Overview
In this role you will support clinical trials as a frontline CRA, ensuring timelines, quality and regulatory compliance across multiple indications. You will build strong site relationships, monitor data integrity and patient safety, and collaborate with cross-functional teams. Based in Barcelona, you contribute to startup activities, data review, and ongoing study progress. This position offers a stable, growth-oriented environment with a focus on professional development and teamwork.

Compensaciones / Ventajas
• Conduct onsite monitoring visits and prepare reports
• Participate in study startup activities
• Perform CRF review, source data verification and query resolution
• Manage site communications and relationships with investigators
• Serve as a point of contact for in-house support and external vendors




• Communicate study progress with internal project teams
• Assist with feasibility research

Responsabilidades
• Life Sciences degree,
• 1 year of experience as a Study Coordinator, or 6 months as a Clinical Research Associate
• Full working proficiency in English and Spanish; fluent in Catalan
• Proficiency in MS Office
• Strong planning, multitasking, and teamwork abilities
• Willingness to travel

Requisitos principales
• Stability, long-term cooperation
• Permanent contract, full-time
• Competitive salary and benefits package
• Career development
• Onboarding courses in clinical research
• Friendly and supportive colleagues

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