Found Description
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...