Job Overview

This full‑time position supports a single sponsor and is based in the Oslo area. The role requires a minimum of two years of clinical monitoring experience, with preference for at least one year of oncology study experience.

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.
• Train site staff to run the study effectively.
• Verify subj...