• Regulatory Operations Manager - Pediatrics

    Dana-Farber Cancer Institute (Boston, MA)
    …(and other institutions' IRBs) + Identify and manage operational, logistical, and regulatory challenges related to the start -up, active, and closeout phases ... relevant to children with cancer and blood disorders. CTIP Regulatory unit will provide pan-CTIP support as part of...proficient knowledge of and ability to execute clinical trials start -up, active and close out phases + Very proficient… more
    Dana-Farber Cancer Institute (12/06/25)
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  • Clinical Trials Regulatory Specialist III…

    Emory Healthcare/Emory University (Atlanta, GA)
    …Coordinate protocol activation/maintenance process and communicates to allow for enrollment to start and maintain once regulatory documents (eg DSMC review) are ... problems and takes a leadership role in resolving. + Lead study start -up/maintenance: prepare and submit all required regulatory documents for new/current… more
    Emory Healthcare/Emory University (11/22/25)
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  • Regulatory Coordinator - Georgetown…

    Georgetown Univerisity (Washington, DC)
    regulatory correspondence and plays a key role in facilitating study start -up and ongoing regulatory maintenance. Strong interpersonal skills are essential, ... a difference in the world. Requirements Job Overview The Regulatory Coordinator plays a critical role in ensuring ...Regulatory Coordinator plays a critical role in ensuring regulatory compliance and oversight of a portfolio of clinical… more
    Georgetown Univerisity (12/13/25)
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  • Regulatory Specialist-CCTO

    Weill Cornell Medical College (New York, NY)
    …when Hired for NYC Offices **Position Summary** Under general direction, oversees the regulatory aspects of clinical trials from start -up through study closeout. ... Title: Regulatory Specialist-CCTO Location: Upper East Side Org Unit: Regulatory Work Days: Monday-Friday Weekly Hours: 35.00 Exemption Status: Non-Exempt Salary… more
    Weill Cornell Medical College (12/10/25)
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  • Regulatory Coordinator

    Georgetown Univerisity (Washington, DC)
    regulatory correspondence and plays a key role in facilitating study start -up and ongoing regulatory maintenance. Strong interpersonal skills are essential, ... a difference in the world. Requirements Job Overview The Regulatory Coordinator plays a critical role in ensuring ...Regulatory Coordinator plays a critical role in ensuring regulatory compliance and oversight of a portfolio of clinical… more
    Georgetown Univerisity (11/21/25)
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  • Associate Clinical Site Lead

    Abbott (Minneapolis, MN)
    …Contracts Associate), as needed. Manage all aspects of study lifecycle to include site regulatory and quality: + Start Up + Nominate, approach, and complete ... aspects of the start -up process and site initiation visits + Understand regulatory and legal requirements for study participation at a level that allows for… more
    Abbott (12/12/25)
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  • Clinical Site Lead - Los Angeles

    Abbott (Pleasanton, CA)
    …as needed. **2. Manage all aspects of study lifecycle to include site regulatory and quality:** Start Up + Nominate, approach, and complete qualification ... aspects of the start -up process and site initiation visits + Understand regulatory and legal requirements for study participation at a level that allows for… more
    Abbott (11/01/25)
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  • THN Program Manager

    University of Washington (Seattle, WA)
    …supervises and partners closely with teams responsible for fiscal management, regulatory affairs, trial start -up, and research coordination. Through strategic ... of research procedures to promote consistency, streamline operations, and ensure regulatory compliance. This position ensures that all research activities, grants,… more
    University of Washington (11/13/25)
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  • Clinical Trial Assistant- Wilmington, DE

    IQVIA (Parsippany, NJ)
    Essential Functions * Assist Clinical Research Associates (CRAs) and Regulatory and Start -Up (RSU) team with accurately updating and maintaining clinical ... coworkers, managers, and clients. * Awareness of applicable clinical research regulatory requirements, ie, Good Clinical Practice (GCP) and International Conference… more
    IQVIA (12/05/25)
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  • Sr. Clinical Research Associate - FSP

    Parexel (Richmond, VA)
    …investigators. + In some countries, as required, CRAs are accountable for study start -up and regulatory maintenance. Tasks may include Site Qualification Visits, ... application process; submission of proper application/documents to EC/IRB and to Regulatory Authorities for start -up and for the duration of the study. + Trains,… more
    Parexel (12/10/25)
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