• Clinical Trial Specialist

    Actalent (Long Branch, NJ)
    Job Title: Clinical Trial Specialist As a Clinical Trial Specialist , you will coordinate the initiation and activation of all new clinical ... is essential. Responsibilities + Coordinate the initiation and activation of clinical trial protocols. + Verify Scientific Review Board, Institutional… more
    Actalent (10/14/25)
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  • Clinical Supply Specialist 2

    ICON Clinical Research (Basking Ridge, NJ)
    Clinical Supply Specialist ICON plc is...vital role in managing the logistics and distribution of clinical trial supplies, ensuring that study sites ... clinical development. We are currently seeking a Clinical Supply Specialist to join our diverse...Doing:** + Managing the planning, procurement, and distribution of clinical trial supplies to study sites. +… more
    ICON Clinical Research (10/04/25)
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  • Clinical Supply Optimization…

    Sanofi Group (Morristown, NJ)
    …than 80 countries so that trial implementation is not disrupted. As a Clinical Supply Optimization Specialist (CSOS) within the CSC-PM team, you will be ... **Job Title:** Clinical Supply Optimization Specialist **Location** :...supplies needed to conduct any Sanofi Pharma and Vaccines clinical trial are set up, planned, ordered,… more
    Sanofi Group (10/15/25)
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  • Lead Pharmacovigilance QC Specialist

    United Therapeutics (Trenton, NJ)
    …experience in pharmacovigilance in either case processing or quality assurance of ICSRs ( clinical trial cases & post-marketing reports), OR + Master's Degree in ... experience in pharmacovigilance in either case processing or quality assurance of ICSRs ( clinical trial cases & post-marketing reports) + 3+ years of experience… more
    United Therapeutics (08/21/25)
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  • Sr. Biologics Sales Specialist (Eastern US)

    Envista Holdings Corporation (Mahwah, NJ)
    **Job Description:** The **Senior Biologics Sales Specialist ** is a hybrid role combining product management and sales support to drive growth of the Implant Direct ... biologics solutions. In addition to regional sales support, the specialist leads downstream marketing initiatives and collaborates cross-functionally with teams… more
    Envista Holdings Corporation (07/30/25)
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  • Senior Specialist , Project Management,…

    Bristol Myers Squibb (New Brunswick, NJ)
    …Oversee the internal packaging and labeling production orders in accordance with the clinical trial design and all relevant regulatory requirements for assigned ... effective management of assigned projects. Manages multiple projects. Liaise with responsible Trial Supply Managers on aspects of clinical supplies packaging and… more
    Bristol Myers Squibb (10/03/25)
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  • Senior Specialist , Quantitative…

    Merck (Rahway, NJ)
    …viral dynamics, model-based meta-analysis, and other model-based analyses + Perform clinical trial simulations to inform dose selection and go/no-go ... of global regulatory expectations of drug and vaccine development, including clinical trial design, clinical pharmacology, biomarker plans, and model-based… more
    Merck (10/09/25)
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  • Patient Recruitment Specialist - US East…

    Parexel (Trenton, NJ)
    **Job Summary:** Parexel is seeking a Patient Recruitment & Retention Specialist to join our dynamic FSP team. This role will be key in supporting the successful ... efforts, and supporting internal and external review / approval clinical & MLR process and related documentation tracking +...study team members to file documents in the electronic Trial Master File (eTMF) for relevant projects according to… more
    Parexel (10/11/25)
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  • Transportation Quality Specialist

    ThermoFisher Scientific (Bridgewater, NJ)
    …ambitious team at the forefront of innovation in transportation, storage, and distribution of Clinical Trial Material. You will be a crucial part of our **Total ... world while building a fulfilling career with us. **Company Information** The Clinical Trials Services Division (CTD) of Thermo Fisher Scientific plays a meaningful… more
    ThermoFisher Scientific (10/15/25)
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  • Senior Principal Regulatory Affairs…

    Bausch + Lomb (Trenton, NJ)
    …ensuring alignment with global requirements. + Provide guidance on risk assessment, clinical trial design implications, and regulatory pathways. + Support ... regulatory strategies for development programs and marketed products across CMC and clinical /non- clinical , labeling, adpromo areas. Serve as a strategic advisor… more
    Bausch + Lomb (09/06/25)
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