Descripción del trabajo
As a Clinical Research Associate I, you support clinical trials across therapeutic indications, ensuring timelines, data quality, and patient safety. You build and maintain relationships with clinical sites and investigators, and oversee monitoring, study startup, and data processes. This office-based role in Barcelona focuses on data integrity, participant rights, and collaboration with multi-disciplinary teams. You contribute to feasibility research and coordinate with vendors and internal teams to drive study progress.
Compensaciones / Ventajas
Conduct and report all types of onsite monitoring visits
Participate in study startup
Perform CRF review, source document verification and query resolution
Responsible for site communication and management
Be a point of contact for in-house support services and vendors




Communicate with internal project teams regarding study progress
Participate in feasibility research
Responsabilidades
College/University degree in Life Sciences
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 applications
Ability to plan, multitask and work in a dynamic team
Ability to travel
Communication, collaboration, and problem-solving skills
Requisitos principales
Stability and long-term cooperation
Permanent contract, full-time
Competitive salary and benefits
Career development
Onboarding courses about clinical research industry
Office in Barcelona
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📌 Clinical Research Associate I (Barcelona)
🏢 PSI Software
📍 Barcelona