At Fortrea, your monitoring work directly protects patients and strengthens the quality of the data that moves trials forward. Join our talent community for upcoming CRA opportunities where you’ll support one sponsor, and help accelerate life‑changing treatments to the people who need them.

These opportunities are for upcoming future roles that may arise at Fortrea. It is a full‑time position supporting a single sponsor and is an excellent opportunity for Study Coordinators and Research Nurses who are looking to transition into a Clinical Research Associate (CRA) role within a CRO. The role is based in the Oslo area.

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.

Summary Of Responsibilities

• Responsible for all aspects of study site monitoring...