• Clinical Research Coord Senior/…

    University of Michigan (Ann Arbor, MI)
    …processes to enhance subject safety during the conduct of all diverse clinical studies. Oversees regulatory documentation for quality assurance. Contributes to ... Qualifications Clinical Research Coordinator Senior: + CRC Governance Committee review and approval + Bachelors degree in Health Science or an equivalent… more
    University of Michigan (11/22/25)
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  • Clinical Research Associate (CRA)

    Vitalief (Phoenix, AZ)
    …+ Strong experience in Remote monitoring/Source document verification (SDV), clinical document review (ie CRFs, monitoring plans, data management plans ... and ensure data accuracy, completeness, and protocol compliance. + Review clinical documentation (eg, CRFs, monitoring plans,...and milestones to ensure alignment with study timelines and quality expectations. + Review and maintain Trial… more
    Vitalief (10/16/25)
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  • Clinical Documentation Auditor

    AdventHealth (Orlando, FL)
    …we are even better. **Schedule:** Full Time **Shift** : Days **Location: Remote ** **The role you'll contribute:** The Clinical Documentation Integrity Manager ... clinical documentation specialists. This role will oversee the review processes of complex patients that vary in age...severity of illness (SOI), risk of mortality (ROM), and quality . + Completes accurate and timely record review more
    AdventHealth (11/14/25)
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  • Behavioral Health Services Manager…

    State of Colorado (Denver, CO)
    …youth within state owned and operated Division of Youth Services facilities. Monitors the quality and quantity of work of the Clinical Directors positions, to ... Behavioral Health Services Manager - Clinical Team Leader for Behavioral Health & Medical...a strong foundation of professional competencies that ensure consistent, high- quality mental health services for detained and committed youth.… more
    State of Colorado (11/20/25)
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  • Clinical Research Coord Assoc- Term-Limited

    University of Michigan (Ann Arbor, MI)
    …manager in establishing data management processes to ensure streamlined systems and high- quality data collection + Review participant requested grocery orders, ... ) + Minimum 2 years of directly related experience in clinical research and clinical trials is necessary. Please review SoCRA's Definition of a Clinical more
    University of Michigan (11/17/25)
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  • Clinical Study Manager

    Takeda Pharmaceuticals (Boston, MA)
    … Operations Program Lead(s): + Oversee the execution of studies in assigned clinical program(s) in compliance with quality standards (including ICH GCP, local ... and empower you to shine? Join us as a Clinical Study Manager based remotely reporting to the ...of the Operational Strategy in preparation for Operational Strategy Review ; focus on ensuring accurate assumptions are applied and… more
    Takeda Pharmaceuticals (11/26/25)
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  • Lead Clinical Study Manager

    Takeda Pharmaceuticals (Boston, MA)
    … Operations Program Lead(s): + Oversee the execution of studies in assigned clinical program(s) in compliance with quality standards (including ICH GCP, local ... empower you to shine? Join us as a Lead Clinical Study Manager based remotely reporting to the ...eg multiple indications, data safety monitoring boards and/or endpoint review committees, interim analyses, requiring the coordination of multiple… more
    Takeda Pharmaceuticals (11/26/25)
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  • Clinical Trials Regulatory Specialist III…

    Emory Healthcare/Emory University (Atlanta, GA)
    …maintains processes and monitors practices to ensure regulatory documentation involving clinical trials complies with Institutional Review Board (IRB) policies ... _Emory Campus-Clifton Corridor_ ** Remote Work Classification** _Hybrid Remote_ **Health and Safety Information** _Position involves clinical patient contact_ more
    Emory Healthcare/Emory University (11/22/25)
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  • Clinical Research Monitor

    General Dynamics Information Technology (Fort Detrick, MD)
    …the continental United States; when required, conduct centralized monitoring activities.** ** Remote review of electronic source documents, electronic Case Report ... in order to identify and mitigate safety and data quality risk issue(s), prepare Clinical Monitoring Reports...and if applicable, other study supplies provided to the clinical sites.** **Prepare and/or review laboratory sample… more
    General Dynamics Information Technology (11/19/25)
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  • Clinical Trials - Clinical Data…

    Lilly (Indianapolis, IN)
    …health challenges. Please note, this is a hybrid position 3 days onsite/2 days remote **Purpose:** This role is responsible for trial level clinical data ... an in depth understanding of data collection, data flow management, data quality , data technology, dataset delivery, archiving and data standards. This role will… more
    Lilly (09/25/25)
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