CRA I, Norway

Job description

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 sposor, and help accelerate life‑changing treatments to the people who need them. This role is for upcoming future opportunities that may arise at Fortrea. It is a full-time position supporting a single sponsor. This 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. Role is based i n 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 including routine monitoring and closeout of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned. - Responsible for all aspects of site management as prescribed in the p...