Pisa Clinical Research Coordinator

3 giorni fa
Pisa, Toscana, Italia IQVIA Tempo pieno
IQVIA is recruiting a Clinical Research Coordinator to support a site in Pisa. This 9h per week role starts immediately and runs for approximately 10-11 months. The role involves prescreening, screening, documentation maintenance (protocols, CRFs, EDC, eTMFs), supporting consent and enrollment, IP-site accountability, and employing IRT/IWRS for randomization and inventory management. Strong IT skills and English fluency are required. #J-18808-Ljbffr

  • Clinical Research Coordinator in Pisa

    3 giorni fa

    pisa, toscana, Italia IQVIA Inc Tempo pieno 45 € Contratto

    Clinical Research Coordinator in Pisa Working Hours: 9 hours per week Start Date : ImmediatelyDuration : Approximately 10-11 months IQVIA is currently recruiting a dedicated Clinical Research Coordinator to support a clinical research site in Pisa. This 9h hour per week role offers a unique opportunity to contribute to meaningful research in a...

  • Part-Time Clinical Research Coordinator

    3 giorni fa

    pisa, toscana, Italia IQVIA Inc Tempo pieno 45 € Contratto

    IQVIA is seeking a Clinical Research Coordinator to support a Pisa-based clinical research site. The role is 9 hours per week with an immediate start and a duration of about 10-11 months. Responsibilities include prescreening, chart reviews, and maintaining critical study documentation in EDC and eTMFs. Ideal candidates hold a life sciences degree, have...

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    Pisa (PI), Provincia di Pisa; Toscana, Italia IQVIA Inc Tempo pieno

    Clinical Research Coordinator in Pisa Working Hours: 9 hours per week Start Date : Immediately Duration : Approximately 10-11 months IQVIA is currently recruiting a dedicated Clinical Research Coordinator to support a clinical research site in Pisa. This 9h hour per week role offers a unique opportunity to contribute to

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    4 giorni fa

    Pisa (PI), Provincia di Pisa; Toscana, Italia IQVIA Inc Part-time

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  • Clinical Research Coordinator

    4 giorni fa

    Pisa (PI), Provincia di Pisa; Toscana, Italia IQVIA Inc Tempo pieno

    Clinical Research Coordinator in Pisa Start Date : Immediately IQVIA is currently recruiting a dedicated Clinical Research Coordinator to support a clinical research site in Pisa. This 9h hour per week role offers a unique opportunity to contribute to meaningful research in a collaborative and dynamic environment. Review charts from the site data...

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    4 giorni fa

    Pisa (PI), Provincia di Pisa; Toscana, Italia IQVIA Inc Tempo pieno

    Clinical Research Coordinator in Pisa Start Date : Immediately IQVIA is currently recruiting a dedicated Clinical Research Coordinator to support a clinical research site in Pisa. This 9h hour per week role offers a unique opportunity to contribute to meaningful research in a collaborative and dynamic environment. Review charts from the site data...

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    3 mesi fa

    Pisa, Toscana, Italia Iqvia Tempo pieno

    Clinical Research Coordinator in PisaWorking Hours:9 hours per weekStart Date: ImmediatelyDuration: Approximately ***** monthsIQVIA is currently recruiting a dedicated Clinical Research Coordinator to support a clinical research site in Pisa. This9h hour per weekrole offers a unique opportunity to contribute to meaningful research in a collaborative and...

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    5 ore fa

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    2 giorni fa

    Pisa, Tuscany, Italia IQVIA Inc Tempo pieno

    Clinical Research Coordinator in Pisa Working Hours: 9 hours per week Start Date: ImmediatelyDuration: Approximately 10-11 months IQVIA is currently recruiting a dedicated Clinical Research Coordinator to support a clinical research site in Pisa. This 9h hour per week role offers a unique opportunity to contribute to meaningful research in a collaborative...

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    3 giorni fa

    Pisa, Tuscany, Italia IQVIA Inc Part-time

    IQVIA is seeking a Clinical Research Coordinator to support a Pisa-based clinical research site. The role is 9 hours per week with an immediate start and a duration of about 10-11 months. Responsibilities include prescreening, chart reviews, and maintaining critical study documentation in EDC and eTMFs.Ideal candidates hold a life sciences degree, have 2–3...

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