• Clinical Trial Specialist

    Actalent (Newark, NJ)
    Job Title: Clinical Trial Specialist Job Description We are seeking a dedicated Clinical Trial Specialist to join our team, focusing on protocol ... role involves collaborating with various departments to initiate and activate new clinical trial protocols, ensuring compliance with regulatory requirements, and… more
    Actalent (01/14/26)
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  • Clinical Contract Documentation…

    Actalent (North Chicago, IL)
    Job Title: Clinical Contract Documentation Specialist IIIJob Description The Clinical Contract Documentation Specialist III will be responsible ... verify patient activity for each agreement, and independently investigate and resolve clinical trial vendor or site payment disputes. Responsibilities + Ensure… more
    Actalent (01/07/26)
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  • Clinical Contract Documentation…

    Actalent (North Chicago, IL)
    …will verify patient activity for each agreement and independently investigate and resolve clinical trial vendor or site payment disputes. Key Responsibilities + ... Investigate and resolve issues independently or with minimal oversight. + Coordinate clinical trial payments to ensure timely processing, including distribution… more
    Actalent (01/08/26)
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  • Sr. EP Field Clinical Specialist

    Abbott (Abbott Park, IL)
    …colleagues serve people in more than 160 countries. **Job Title** Sr. EP Field Clinical Specialist - Central/Western US **Working at Abbott** At Abbott, you can ... are seeking an experienced, high caliber Senior EP Field Clinical Specialist . This position will be primarily...therapy area. + Serve as a technology, protocol and clinical trial procedure expert and resource Abbott… more
    Abbott (11/29/25)
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  • Senior Specialist , Clinical

    Edwards Lifesciences (Kansas City, KS)
    …exam results for consistency with case report form, and determine if clinical trial /study subject documentation is within parameters of study hypothesis, ... as well as to monitor clinical trial /study safety, in keeping with protocols, GCP (Good Clinical Practices) and regulatory requirements + Develop and deliver… more
    Edwards Lifesciences (11/14/25)
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  • Clinical Supply Specialist

    Actalent (Alameda, CA)
    …packaging projects, including oversight of CMO scheduling, production of labels, and packaging of clinical trial supplies. + Review clinical trial ... Job Title: Clinical Supply SpecialistJob Description The Clinical Supply Specialist plays a pivotal role...ensure compliance with US and international regulations. + Represent clinical supplies function at clinical trial more
    Actalent (01/07/26)
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  • Clinical Production Specialist - 2nd…

    Catalent Pharma Solutions (Philadelphia, PA)
    …of Clinical , contract or production experience required + Clinical Trial Manufacturing and Packaging experience preferred + Computer literate (Microsoft ... ** Clinical Production Specialist ** **Position Summary:** +...organizes and performs all functions associated with packaging of clinical trial supplies and assures compliance to… more
    Catalent Pharma Solutions (01/07/26)
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  • Field Clinical Specialist

    Abbott (Abbott Park, IL)
    …generic medicines. Our 114,000 colleagues serve people in more than 160 countries. **Field Clinical Specialist ** **Working at Abbott** At Abbott, you can do work ... device and management solutions for treating structural heart disease. As the **Field Clinical Specialist ** , along with your leadership team you will plan… more
    Abbott (12/04/25)
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  • Senior Clinical Trials Specialist

    SUNY Upstate Medical University (Syracuse, NY)
    Job Summary: The Senior Clinical Trials Contract Specialist will be the point of contact for review, preparation, processing, and negotiation of Clinical ... regulations, and sponsor requirements, collaborate with legal, hospital finance, and clinical operations teams to resolve contract issues and discrepancies.… more
    SUNY Upstate Medical University (12/13/25)
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  • Grants and Contracts Manager/ Specialist

    University of Washington (Seattle, WA)
    …review of all documents and data related to the clinical trial funding, including study budget, protocol, contract , and other supporting documentation. ... from the implementation and integration of Workday Finance. The Grant and Contract Specialist is responsible for reviewing contractual materials for accuracy… more
    University of Washington (11/21/25)
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  • Research Specialist - Coverage Analyst

    UPMC (Pittsburgh, PA)
    Purpose: The Clinical Trial Coverage Analyst is responsible for ensuring the billing compliance and proper coverage of clinical trial procedures. This ... role involves reviewing clinical trial protocols to determine what is billable to third-party...that should be covered by the study sponsor. The specialist collaborates with clinical research teams, finance… more
    UPMC (12/19/25)
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  • Biomedical Equipment Support Specialist

    Veterans Affairs, Veterans Health Administration (Hot Springs, SD)
    Summary The Biomedical Equipment Support Specialist (BESS) provides clinical and administrative support to staff, patients, and administrators for all matters of ... to, the following: Manages the lifecycle of medical equipment and clinical systems. Functions include: technology assessment including defining requirements and… more
    Veterans Affairs, Veterans Health Administration (12/11/25)
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  • Biomedical Equipment Support Specialist

    Veterans Affairs, Veterans Health Administration (Indianapolis, IN)
    Summary The Biomedical Equipment Support Specialist (BESS) provides clinical and administrative support to staff, patients, and administrators for all matters of ... but are not limited to: Lifecycle management of all medical devices and clinical systems to include physical and network support. Coordinates and works effectively… more
    Veterans Affairs, Veterans Health Administration (01/04/26)
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  • OnCore Financial (Post-Award) Specialist

    UPMC (Pittsburgh, PA)
    …visit. The specialist maintains and adjusts financial data within the clinical trial management systems (CashFlow/OnCore) and ensures alignment with UPMC's ... and manage sponsor invoicing to ensure timely payment for clinical trial activities + Reconcile payments based...compliance + Track revenue and maintain payment logs for clinical trials + Coordinate contract closeouts and… more
    UPMC (12/19/25)
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  • Supervisory Biomedical Equipment Support…

    Veterans Affairs, Veterans Health Administration (Detroit, MI)
    Summary Serves as a Supervisory Biomedical Equipment Support Specialist (BESS) within the Biomedical Engineering Section of Facilities Management Service at the John ... Responsibilities The major duties of the Supervisory Biomedical Equipment Support Specialist (BESS) include, but are not limited to: Oversees, directs, and… more
    Veterans Affairs, Veterans Health Administration (01/07/26)
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  • Biomedical Equipment Support Specialist

    Veterans Affairs, Veterans Health Administration (Syracuse, NY)
    Summary The Biomedical Equipment Support Specialist provides clinical and administrative support to staff, patients, and administrators for all matters of ... provided by staff throughout VA. Responsibilities The Biomedical Equipment Support Specialist provides clinical and administrative support to staff, patients,… more
    Veterans Affairs, Veterans Health Administration (11/19/25)
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  • Research and Operations Specialist

    Kelly Services (Colorado Springs, CO)
    Kelly(R) Science & Clinical is seeking an R&D Specialist for a contract -to-hire opportunity with one of our clients, a leading small molecule CDMO at their ... Experts. **Workplace:** Onsite in Colorado Springs, CO **Position Title:** R&D Specialist **Position Type:** Contract -to-hire **Pay rate:** $32-36/hour **R&D … more
    Kelly Services (01/10/26)
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  • Oncology CRA/ Clinical Site Monitor…

    Astellas Pharma (New York, NY)
    Clinical Trial Lead (CTL,) Clinical Trial Manager (CTM,) Clinical Trial Specialist (CTS,) and Study Start-Up Specialist (SSS) to ensure ... trial sites to ensure inspection readiness through compliance with the clinical trial protocol, company Standard Operating Procedures (SOP), Good Clinical more
    Astellas Pharma (01/13/26)
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  • Clinical Research Budget Analyst

    University of Washington (Seattle, WA)
    …Analyst position is responsible for developing and negotiating budgets and payment terms of clinical trial agreements for clinical trials and clinical ... budgets and performing negotiations with industry biotech and biopharma sponsors on complex clinical trial protocols while adhering to aggressive trial more
    University of Washington (12/03/25)
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  • Supervisory Supply Management Specialist

    Veterans Affairs, Veterans Health Administration (Washington, DC)
    Summary This position serves as the Supervisory Logistics Management Specialist - Chief Supply Chain Officer responsible for the development and integration of a ... Responsibilities Duties: This position serves as the Supervisory Supply Management Specialist - Chief Supply Chain Officer responsible for the development and… more
    Veterans Affairs, Veterans Health Administration (01/02/26)
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