Clinical Research Associate – Italy: Site Monitoring

A leading global provider of clinical research services is seeking an Entry-level Clinical Research Associate in Milan, Italy. The role involves conducting clinical monitoring visits, managing study processes, and ensuring adherence to regulatory requirements. Candidates should possess a Bachelor's degree in a scientific discipline and have communication...

A clinical research services firm is seeking a Clinical Research Associate in Milan, Italy. This position involves conducting site monitoring visits, ensuring compliance with regulations, and maintaining study documentation. A Bachelor's degree in a scientific discipline or healthcare, along with at least one year of clinical experience, is preferred. The...

Clinical Research Associate, Site Management - ItalyJob OverviewEngage in a structured training program to gain the knowledge and skills required to independently conduct clinical monitoring visits in accordance with the study protocol, standard operating procedures, good clinical practice, and applicable regulatory requirements.Essential FunctionsComplete...

A clinical research organization is seeking a full-time Clinical Research Associate to join their monitoring team in Italy. Responsibilities include conducting site visits for compliance, communicating with medical staff, and verifying investigator qualifications. Candidates should have a Master's degree in a health-related field, CRA certification, and...

Clinical Research Associate, Site Management - Italy Engage in a structured training program to gain knowledge and skills required to independently conduct clinical monitoring visits in accordance with study protocol, standard operating procedures, good clinical practice, and applicable regulatory requirements.Essential FunctionsComplete appropriate...

Clinical Research Associate, Site Management - ItalyEngage in a structured training program to gain knowledge and skills required to independently conduct clinical monitoring visits in accordance with study protocol, standard operating procedures, good clinical practice, and applicable regulatory requirements.Essential FunctionsComplete appropriate...

Clinical Research Associate, Site Management - ItalyEngage in a structured training program to gain knowledge and skills required to independently conduct clinical monitoring visits in accordance with study protocol, standard operating procedures, good clinical practice, and applicable regulatory requirements.Essential FunctionsComplete appropriate...

A leading global clinical research provider is seeking an experienced Clinical Research Associate to perform monitoring and site management work. Responsibilities include site visits, ensuring compliance with study protocols, and managing study progress. Candidates should hold a Bachelor's and Master's degree in a relevant field, possess CRA Certification,...

Clinical Research Associate, Sponsor Dedicated - Italy Get AI-powered advice on this job and more exclusive features.Responsibilities Perform site selection, initiation, monitoring and close-out visitsSupport the development of a subject recruitment planEvaluate the quality and integrity of site practices in accordance with regulatory requirements, i.e.,...

Clinical Research Associate, Sponsor Dedicated – ItalyJoin to apply for the Clinical Research Associate, Sponsor Dedicated – Italy role at IQVIAResponsibilitiesPerforming site selection, initiation, monitoring and close‑out visitsSupporting the development of a subject recruitment planEvaluating the quality and integrity of site practices in accordance...