Experteer Overview

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In this CRA role you support clinical trial execution across site qualification, initiation, monitoring, and close-out visits to drive high-quality data and patient safety. You will mentor junior staff, assess protocol adherence, and ensure accurate documentation in TMF. Your work directly contributes to reliable trial results and patient care, within a collaborative, value-driven culture.

This position offers hands-on field exposure, cross-functional collaboration, and opportunities to shape site performance on meaningful studies.

Compensaciones / Ventajas

- Site qualification, initiation, interim monitoring, and close-out visits
- Mentor and guide less experienced CRAs and site staff
- Document site visit findings via reports
- Train site staff on protocol adherence as required
- Review study subject safety information and informed consent




- Perform source data verification for data integrity and patient safety
- Review CRFs in paper or electronic systems and resolve data queries
- Provide updates for TMF filing
- Ensure IP receipt, accountability and destruction compliance
- Conduct accompanied site visits for assessment or training of other CRAs

Responsabilidades

- 5+ years of experience as a Clinical Research Associate
- xugodme 4-year university degree or RN/BSN in Nursing
- Willingness to travel
- Excellent interpersonal, oral, and written communication skills in English
- Strong organizational skills and attention to detail
- Ability to work with little or no supervision
- Proficiency in Microsoft Office, CTMS and EDC Systems

Requisitos principales

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Hay opciones de teletrabajo/trabajo desde casa disponibles para este puesto.

📌 Senior Clinical Research Associate - Spain - Remote (Barcelona)
🏢 Worldwide Clinical Trials
📍 Barcelona