21 ago
|
Fortrea
|
Madrid
Fortrea is seeking a Clinical Research Associate to oversee site monitoring and management for clinical studies in accordance with SOPs and regulatory guidelines. The role involves ensuring patient safety, data integrity, and adherence to study plans while collaborating with vendors and internal teams.
Responsibilities include site initiation and closeout visits, source data verification, and regulatory submissions coordination.
📌 Clinical Research Associate I: Site Monitor (Madrid)
🏢 Fortrea
📍 Madrid