• Ancillary Supplies Coordinator

    ICON Clinical Research (NC)
    …you will play a key role in overseeing the management and distribution of clinical trial supplies, ensuring that all materials are delivered efficiently and in ... **What You Will Be Doing:** + Managing the end-to-end supply chain for clinical trial materials, including planning, procurement, and distribution to ensure… more
    ICON Clinical Research (12/07/25)
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  • Principal Biostatistician FSP, Neuroscience

    IQVIA (Durham, NC)
    …to establish project objectives and timelines. + Write the statistical sections of clinical trial protocols, while consulting with internal and external experts. ... field with 7+ years of industry experience. + **At least 3 years in clinical trial experience in phase 2 and 3 plus 2 years in observational/RWE studies.** +… more
    IQVIA (12/02/25)
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  • Regional Sales Director, Structural Heart - TAVI…

    Abbott (Charlotte, NC)
    … sales specialist to develop a high performing team for commercial and clinical trial activity responsibilities. The RSD will meet the authorization training ... and organizational objectives specifically, marketing, training, enterprise accounts and clinical trial . + Demonstrates exceptional organizational and… more
    Abbott (11/25/25)
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  • Regional Sales Director, CRM - San Francisco/Bay…

    Abbott (San Francisco, CA)
    clinical specialist to develop a high performing team for commercial and clinical trial activity responsibilities. The RSD will meet the authorization ... and organizational objectives specifically, marketing, training, enterprise accounts and clinical trial . + Demonstrates exceptional organizational and… more
    Abbott (11/18/25)
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  • Research Coordinator I - Gastroenterology

    Dartmouth Health (Lebanon, NH)
    …other research staff and is involved at a fundamental level to support basic administrative clinical trial tasks. The Clinical Research Coordinator I has no ... such as subject visit preparation, performs data entry in the Clinical Trial Management System (CTMS), scans informed consents into Electronic Medical Record… more
    Dartmouth Health (10/28/25)
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  • Research Data Specialist - Thoracic Oncology

    Dana-Farber Cancer Institute (Boston, MA)
    …+ Responsible for data entry of Subject Visit Tracking information into Clinical Trial Management System contemporaneously with medical visits, assessments, and ... and effort spent on study-specific activities and other administrative tasks into Clinical Trial Management System contemporaneously with work completed. +… more
    Dana-Farber Cancer Institute (10/23/25)
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  • Medical Director, Product Development, CVRM

    Genentech (Boston, MA)
    …and clinical experience + You have 2+ years of post-grad relevant clinical /scientific research and/or clinical trial experience + You have significant ... drug development process. + You have demonstrated experience working with various clinical trial designs, (eg accelerated approval, pivotal, breakthrough etc) +… more
    Genentech (10/17/25)
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  • Department Director of Research Operations…

    Dartmouth Health (Lebanon, NH)
    …operations at Dartmouth-Hitchcock at the Department or Center level, encompassing research compliance, clinical trial contracting, and clinical trial ... databases and general computing software is essential, and experience with clinical trial management system is desired. Required Licensure/Certifications -… more
    Dartmouth Health (10/08/25)
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  • Research Nurse

    Catholic Health Services (West Islip, NY)
    …Nurse Specialist- Cancer Services Job Duties: + Coordinates the day-to-day management of clinical trial , ensuring that the study is conducted in accordance with ... + Screens patients to determine if appropriate for enrollment in clinical trial , maintain screening logs, complete inclusion-exclusion eligibility, obtain… more
    Catholic Health Services (10/03/25)
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  • Senior Specialist, Global Trade Compliance

    Takeda Pharmaceuticals (Cambridge, MA)
    …of export and import compliance policies and procedures for the organization regarding Clinical Trial Material (CTM) and raw material shipments. + Manage daily ... Ensure adherence to country specific standard operating procedures for importing/exporting clinical trial material and raw materials, including logistics,… more
    Takeda Pharmaceuticals (12/12/25)
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