Job Summary

At Fortrea, your monitoring work directly protects patients and strengthens the quality of the data that moves trials forward. This full‑time position supports a single sponsor and is based in the Oslo area. It is an excellent opportunity for Study Coordinators and Research Nurses looking to transition into a Clinical Research Associate (CRA) role within a CRO.

Job Overview

Site monitoring and site management responsibility for clinical studies according to Company and/or Sponsor Standard Operating Procedures and Regulatory Guidelines. Assures the implementation of project plans as assigned.

Responsibilities

• Responsible for all aspects of study site monitoring, including routine monitoring, closeout of clinical sites, maintenance of study files, and conduct of pre‑study and initiation visits.
• Responsible for all aspects of site management as prescribed in the project plans.
• Ensure the study staff receive ...