Location
oslo, oslo, Norway
Posted
July 24, 2026
Job 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 report...
**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 report...