Experteer Overview 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 / Incentivos
- 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 researchResponsabilidades
- 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 skillsRequisitos 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

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