Remote CRA: Clinical Trials Monitoring

1 settimana fa


Via Milano, Italia IQVIA A tempo pieno

A leading global provider of clinical research services is seeking an Experienced Clinical Research Associate to monitor and manage clinical study sites based in Italy. The ideal candidate will have a Bachelor's degree and a Master's degree in a scientific field or health care, along with CRA certification. The role involves ensuring regulatory compliance, managing documentation, and maintaining effective site communication. Candidates should be organized, fluent in English, and able to travel if necessary. This contract position offers opportunities for growth and involvement in healthcare innovations.#J-18808-Ljbffr



  • Via Milano, Italia ICON A tempo pieno

    A leading clinical research organization is seeking a Clinical Research Associate II or Senior CRA in Italy. This role involves independently monitoring clinical trials, managing study documentation, and mentoring junior staff. The ideal candidate will have a life sciences degree and relevant experience, along with fluency in French and professional English....


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    A leading clinical research organization is seeking a Clinical Research Associate II or Senior CRA in Italy. This role involves independently monitoring clinical trials, managing study documentation, and mentoring junior staff. The ideal candidate will have a life sciences degree and relevant experience, along with fluency in French and professional English....


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    A leading clinical research organization is seeking a Clinical Research Associate II or Senior CRA in Italy.This role involves independently monitoring clinical trials, managing study documentation, and mentoring junior staff.The ideal candidate will have a life sciences degree and relevant experience, along with fluency in French and professional...

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  • Milano, Italia ICON A tempo pieno

    A leading clinical research organization is seeking a Clinical Research Associate II or Senior CRA in Italy. This role involves independently monitoring clinical trials, managing study documentation, and mentoring junior staff. The ideal candidate will have a life sciences degree and relevant experience, along with fluency in French and professional English....


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