Clinical Research Associate Professional

2 weeks ago


kwai tsing district, Hong Kong SAR China IQVIA Argentina Full time

Job Overview

We are seeking a highly skilled Clinical Research Associate to join our team at IQVIA Argentina. As a key member of our team, you will be responsible for ensuring that study sites conduct the study and report data as required by the study protocol, regulations, and sponsor requirements.



  • kwai tsing district, Hong Kong SAR China IQVIA Argentina Full time

    About the RoleWe are seeking a highly skilled Clinical Research Associate to join our team at IQVIA Argentina. As a Clinical Research Associate, you will be responsible for conducting site management and monitoring visits to ensure that sites are conducting clinical trials in accordance with contracted scope of work and regulatory requirements.Key...


  • kwai tsing district, Hong Kong SAR China IQVIA Argentina Full time

    Job Overview">At IQVIA, we are seeking a highly skilled Clinical Research Associate to join our team. As a key member of our site management team, you will be responsible for ensuring the smooth conduct of clinical trials at our partner sites.">We are looking for a professional with strong knowledge of Good Clinical Practice (GCP) and International...


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    Job OverviewClinical Research Associates play a pivotal role in ensuring the success of clinical trials by conducting site monitoring visits, managing study data, and adhering to regulatory requirements. This position involves working closely with sites to adapt and drive subject recruitment plans, administer protocol training, and evaluate site...


  • Kwai Tsing District, Hong Kong SAR China IQVIA Argentina Full time

    Job OverviewPerform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.Essential FunctionsPerform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with...


  • kwai tsing district, Hong Kong SAR China IQVIA Argentina Full time

    Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with...


  • Kwai Tsing District, Hong Kong SAR China IQVIA Argentina Full time

    Job OverviewAs a Clinical Research Associate at IQVIA Argentina, you will be responsible for ensuring that sites conducting clinical studies are following Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.Key ResponsibilitiesPerform site monitoring visits to assess compliance with study protocols and regulatory...


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  • Kwai Tsing District, Hong Kong SAR China IQVIA Argentina Full time

    Job DescriptionWe are looking for an experienced Clinical Research Associate to join our team at IQVIA Argentina. The successful candidate will be responsible for ensuring the quality and integrity of clinical trials conducted at our partner sites.ResponsibilitiesPerform site initiation, monitoring, and close-out visits to ensure compliance with study...


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    About the RoleAs a Clinical Research Associate, you will be responsible for performing site monitoring visits, tracking regulatory submissions, and managing study data. You will work closely with sites to develop and implement subject recruitment plans and ensure compliance with Good Clinical Practice (GCP) and International Conference on Harmonization (ICH)...


  • kwai tsing district, Hong Kong SAR China IQVIA Argentina Full time

    Site Monitoring and Management RoleWe are seeking an experienced Clinical Research Associate to join our team at IQVIA Argentina. As a key member of our clinical operations team, you will be responsible for ensuring the smooth conduct of clinical trials at research sites across the country.Your Key Responsibilities Will Include:Conducting site initiation,...


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  • Research Monitor

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    kwai tsing district, Hong Kong SAR China IQVIA Argentina Full time

    About the Position">This Clinical Research Associate role is a key position within our site management team. The successful candidate will be responsible for ensuring the smooth conduct of clinical trials at our partner sites.">You will be responsible for performing monitoring and site management work to ensure compliance with Good Clinical Practice (GCP)...


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