Fortrea seeks a Clinical Research Associate II with general medicine experience to conduct clinical site monitoring, ensure regulatory compliance, and manage data quality for studies in Galicia. This is a permanent position reporting to the FSP team.

Responsibilities

- Conduct routine, pre-study, initiation, and close-out site visits with full protocol compliance
- Verify source documents, review case report forms, and manage data queries for accuracy
- Track serious adverse events and support safety reporting and narrative preparation
- Prepare trip reports, maintain audit readiness, and coordinate study materials and vendors
- Perform feasibility assessments, quality control visits, and provide local project coordination

Requirements

- University degree in scientific or medical field
- Minimum 2 years independent monitoring experience in general medicine
- Thorough knowledge of ICH GCP Guidelines and Spanish regulatory requirements
- Fluent in Spanish and English, written and verbal
- Valid driver's license
- Proficiency with standard computer applications

📌 Clinical Research Associate II (España)
🏢 Fortrea
📍 España