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Fortrea seeks an experienced Clinical Research Associate II for Italy to oversee site monitoring and site management for multicenter studies. You will ensure adherence to regulatory guidelines, manage study files, and support initiation and closeout visits with vendors and sponsors.
The role involves implementing project plans, ensuring quality deliverables, and maintaining regulatory compliance across sites in Italy. Strong communication and documentation skills are essential for success.
Fortrea Research Associate
PostedAug 2026
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 as…