Clinical Research Associate – Italy: Site Monitoring

6 giorni fa


Milano, Italia Iqvia A tempo pieno

A leading global provider of clinical research services is seeking a Clinical Research Associate in Milan.The role involves conducting site selection, initiation, monitoring, and close-out visits.Candidates must possess a Bachelor's and Master's degree in a scientific discipline, along with CRA certification.Excellent English skills and flexibility to travel are essential.This full-time position offers a supportive work environment and an attractive benefits package, including a company car and mobile phone.#J-*****-Ljbffr



  • Milano, Italia IQVIA A tempo pieno

    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...


  • Milano, Italia IQVIA A tempo pieno

    Clinical Research Associate, Site Management - Italy Join to apply for the Clinical Research Associate, Site Management - Italy role at IQVIA . Engage in a structured training program to acquire the knowledge and skills necessary to independently conduct clinical monitoring visits in accordance with study protocols, standard operating procedures, good...


  • Milano, Italia IQVIA A tempo pieno

    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...


  • Milano, Italia IQVIA A tempo pieno

    A leading global provider of clinical research services is seeking a Clinical Research Associate in Milan. The role involves conducting site selection, initiation, monitoring, and close-out visits. Candidates must possess a Bachelor's and Master's degree in a scientific discipline, along with CRA certification. Excellent English skills and flexibility to...


  • Milano, Italia Iqvia A tempo pieno

    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...


  • Milano, Italia Iqvia A tempo pieno

    A leading global clinical research provider in Milan is seeking a Clinical Research Associate for an entry-level contract position.Responsibilities include conducting site monitoring visits and ensuring regulatory compliance in clinical trials.Ideal candidates will have a Bachelor's degree, prior clinical experience is preferred, along with strong...


  • Milano, Italia Iqvia A tempo pieno

    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 ideal...


  • Milano, Italia IQVIA A tempo pieno

    Clinical Research Associate, Site Management - Italy Job Overview Engage 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 Functions...


  • Milano, Italia Iqvia A tempo pieno

    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...


  • Milano, Italia Iqvia A tempo pieno

    Clinical Research Associate, Site Management - Italy2 days ago.Be among the first 25 applicants.Job 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...