Position

Clinical Research Associate (CRA), full‑time, home‑based in Barcelona and surrounding areas.

Travel up to 60‑80%.

About the Role

As a CRA you will conduct site qualification, initiation, monitoring, and close‑out visits in compliance with approved protocols. You will communicate with site staff, verify investigator qualifications and resources, and audit records against source documents. You will review regulatory documents, manage investigational product inventory, verify adverse events, and assess recruitment and retention success. Monitoring reports will be completed and follow‑up letters sent to secure compliance.

• Conduct qualification, initiation, monitoring, and close‑out visits for research sites.
• Communicate with site staff, including coordinators, physicians, and other personnel.
• Verify investigator qualifications, training, and resources.
• Validate medical records and source documentation ver...