• Senior Clinical Research

    Avania (OR)
    …the key role of experienced Clinical Research Associate ( CRA ) or Senior Clinical Research Associate ( Sr CRA ) As a CRA / Sr ... for several studies running in parallel, in all associated clinical trial phases, from regulatory submissions to...of relevant work experience as a clinical research associate - CRA . +… more
    Avania (05/15/25)
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  • Senior CRA / CRA II

    ICON Clinical Research (Portland, OR)
    …to shape the future of clinical development. We are currently seeking a Senior Clinical Research Associate ( CRA ) or CRA II to join our ... Senior CRA / CRA ...the study lifecycle. **What You Will Be Doing:** + Monitoring clinical trial sites to...sciences, nursing, or medicine. + Extensive experience as a Clinical Research Associate , with a… more
    ICON Clinical Research (06/24/25)
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  • Senior Clinical Site Manager…

    Astellas Pharma (Northbrook, IL)
    trial sites to ensure inspection readiness through compliance with the clinical trial protocol, company Standard Operating Procedures (SOP), Good Clinical ... will manage the site/sponsor relationship as it relates to clinical trial delivery through consistent communication and...used for trial management. + Fully documents trial related activities, in particular monitoring . Writes… more
    Astellas Pharma (06/21/25)
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  • Clinical Research Associate I

    Abbott (Alameda, CA)
    …new sensing technology. The CRA will ensure quality, accuracy, and integrity of clinical trial data throughout the full lifecycle of multiple clinical ... senior staff in development of study-specific forms and trial -specific monitoring plans. + Assist senior...sciences preferred or equivalent with minimum 2 years of clinical research experience, or combination of appropriate… more
    Abbott (06/04/25)
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  • Clinical Research Associate I

    Abbott (Alameda, CA)
    …**The Opportunity:** The CRA will ensure quality, accuracy, and integrity of clinical trial data throughout the full lifecycle of multiple clinical ... senior staff in development of study-specific forms and trial -specific monitoring plans. + Assist senior...preferred or equivalent with minimum one (1) year of clinical research experience, or combination of appropriate… more
    Abbott (06/04/25)
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  • Sr . CRA , Sponsor Aligned, Oncology

    IQVIA (Overland Park, KS)
    Job Overview: Join our dynamic team as a Clinical Research Associate ! You'll play a pivotal role in monitoring and managing clinical trial sites ... we'd love to hear from you! IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life… more
    IQVIA (05/06/25)
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  • Sr . CRA / CRA 2, Oncology,…

    IQVIA (Durham, NC)
    …applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement. ... **IQVIA is seeking a Sr . CRA 1 or CRA.... \#CRAFSAJD IQVIA is a leading global provider of clinical research services, commercial insights and healthcare… more
    IQVIA (06/17/25)
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  • Senior Clinical Research

    BeOne Medicines (San Mateo, CA)
    …**Essential Functions of the job:** * Perform and coordinate assigned aspects of the clinical monitoring process in accordance with GCPs and SOPs to assess the ... collection is met per contractual guidelines * Works with Clinical Trial Oversight Managers (CTOMs) and ... Operations experience * Minimum of 3-4 years of ( CRA ) monitoring experience in the pharmaceutical or… more
    BeOne Medicines (04/23/25)
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  • Clinical Research Associate

    Abbott (Alameda, CA)
    …to clinical sites and performing study device accountability. + Manage clinical monitoring activities and overall site management ensuring compliance to the ... life sciences or equivalent with minimum 5 years of clinical research experience + Must have 2+...management. + Solid understanding and demonstrated experience of the clinical trial process including study design and… more
    Abbott (05/31/25)
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  • ( Senior ) Clinical Research

    IQVIA (Parsippany, NJ)
    …applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement. ... required study documentation. * Act as a mentor for clinical staff including conducting co- monitoring and training...In depth knowledge of, and skill in applying, applicable clinical research regulatory requirements, ie, Good … more
    IQVIA (04/14/25)
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