Lavori attuali relativi a Senior Cra – Remote - GENOVA - Letuelezioni

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  • Senior CRA

    1 settimana fa


    Genova, Italia Hitachi Automotive Systems Americas, Inc. A tempo pieno

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    Social network you want to login/join with:Senior Clinical Research Associate, genovacol-narrow-leftClient:TeleflexLocation:Job Category:Other-EU work permit required:Yescol-narrow-rightJob Reference: Job Views:2Posted: Expiry Date: col-wideJob Description:POSITION SUMMARY:The Senior Clinical Research Associate (Senior CRA) is responsible for scheduling and...


  • genova, Italia Hitachi Automotive Systems Americas, Inc. A tempo pieno

    POSITION SUMMARYThe Senior Clinical Research Associate (Senior CRA) is responsible for scheduling and conducting on-site and remote monitoring visits in compliance with applicable regulatory standards (MDR, ISO 14155, ICH/GCP guidelines, Teleflex procedures and IRB/EC policies and procedures). The Senior CRA conducts monitoring visits as identified by the...


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    Social network you want to login/join with:Senior Clinical Research Associate, genovacol-narrow-leftClient:TeleflexLocation:Job Category:Other-EU work permit required:Yescol-narrow-rightJob Reference:855679022200258560033717Job Views:2Posted:**********Expiry Date:**********col-wideJob Description:POSITION SUMMARY:The Senior Clinical Research Associate...


  • Genova, Italia Letuelezioni A tempo pieno

    POSITION SUMMARY The Senior Clinical Research Associate (Senior CRA) is responsible for scheduling and conducting on-site and remote monitoring visits in compliance with applicable regulatory standards (MDR, ISO 14155, ICH/GCP guidelines, Teleflex procedures and IRB/EC policies and procedures). The Senior CRA conducts monitoring visits as identified by the...

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Senior Cra – Remote

7 ore fa


GENOVA, Italia Letuelezioni A tempo pieno

A leading clinical research organization is seeking a Senior Clinical Research Associate to conduct on-site and remote monitoring visits.This role requires a minimum of 5 years of experience in clinical trial monitoring, alongside proficiency in ICH/GCP guidelines.The ideal candidate will demonstrate excellent attention to detail, organizational skills, and effective communication abilities.Responsibilities include evaluating data accuracy, preparing monitoring visit reports, and collaborating with clinical site staff to ensure compliance and quality standards are met.#J-*****-Ljbffr