This role is for upcoming future opportunities that may arise at Fortrea. It is a full-time position supporting a single sponsor. Role is based in the Oslo area.

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 docu...