CRA II, Denmark

Job description

This role is for upcoming future opportunities that may arise at Fortrea. Join Fortrea as a CRA – exciting future opportunities across multiple sponsors We’re excited to invite CRAs to join Fortrea, where you’ll work on a diverse portfolio of studies across multiple sponsors. This role offers strong exposure to different therapeutic areas, high-quality standards, and the opportunity to further develop your monitoring expertise in a global environment. Key requirement: Minimum 2 years of clinical monitoring experience Preferably 1+ year experience in oncology studies Summary of Responsibilities: Manage clinical trial sites in line with Fortrea SOPs, ICH GCP and sponsor requirements Perform all monitoring visits (PSV, SIV, routine, close-out) Ensure patient safety by verifying informed consent and protocol adherence Maintain data integrity through SDV, query management, and data review Keep site regulatory documentation and eTMF up to date Oversee investigational product handling, storage, and accountability Ensure audit readiness and compliance with quality standards and CRA metrics Prepare monitoring plans, visit reports, and study documentation On-site Monitoring Responsibilities:...