Worldwide Clinical Trials seeks a Senior Clinical Research Associate based in Barcelona to oversee clinical trial site activities including qualification, initiation, monitoring, and closeout. This remote-eligible role requires managing protocol compliance, staff training, and data integrity across multiple study sites.
Responsibilities
- Conduct site qualification, initiation, monitoring, and closeout visits
- Mentor junior CRAs and site staff; assess and train on protocol adherence
- Verify source documents and review case report forms for data accuracy
- Document site visit findings and resolve data queries with sites
- Manage investigational product accountability and Trial Master File documentation

Requirements
- 5+ years experience as a Clinical Research Associate
- 4-year university degree or RN/BSN in Nursing
- Fluent English with excellent written and oral communication
- Proficiency in Microsoft Office, CTMS, and EDC systems
- Superior organizational skills with meticulous attention to detail
- Ability to work independently with minimal supervision
- Willingness to travel as required

📌 Senior Clinical Research Associate (España)
🏢 Worldwide Clinical Trials
📍 España