• Associate Director Finance Operations (HYBRID…

    Charles River Laboratories (Malvern, PA)
    …present financials and key indicators to senior leadership for business reviews, management reporting, budget and strategic planning. * Prepare analysis of monthly, ... internal business partners, providing financial expertise on processes and value-added management to support them in achieving their objectives, including but not… more
    Charles River Laboratories (09/17/25)
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  • Clinical Research Leader (PM) - Jjmt…

    J&J Family of Companies (Irvine, CA)
    …CDE, GCP, ISO 14155, MDR, MEDDEV). + Medical device experience highly preferred. + CRO experience and site management and clinical site monitoring are assets. + ... May serve as the primary contact for clinical trial sites (eg site management ); + Develops clinical trial documents (eg study protocol, informed consents, CRF,… more
    J&J Family of Companies (09/16/25)
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  • Histology Supervisor

    Charles River Laboratories (Horsham, PA)
    …planning and scheduling of laboratory projects. * Assist pathology management in ensuring sufficient and appropriate resources (personnel, equipment, facilities, ... available to perform laboratory procedures. * Responsible for personnel management activities such as: scheduling, personnel actions (hiring, promotions, transfers,… more
    Charles River Laboratories (09/12/25)
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  • Director, Health Research Operations

    Meta (Burlingame, CA)
    …Scientist Leads, collaborate with relevant interdisciplinary functions (Product Management , Engineering, Hardware teams,Regulatory/Compliance as needed) to ensure ... operations) to execute internal and external studies end to end, spanning CRO /vendors selection, site selection and qualification, study documents and manuals, IRB,… more
    Meta (09/12/25)
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  • Associate Director Production Quality

    Charles River Laboratories (Rockville, MD)
    …and corrective actions, and line clearances. + Develop and execute training and Management briefings at any technical or compliance level required on updates and ... to and ensure necessary Quality oversight to areas within span of control . + Effectively model, demonstrate and live an employee-focused leadership style that… more
    Charles River Laboratories (09/11/25)
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  • Senior Principal Product Leader, Integrated…

    Genentech (South San Francisco, CA)
    …Data domain provides the end-to-end digital backbone for research design, experiment management , assay data & insights, and integrated research solutions. It spans ... requirements:** + 10+ years of product leadership in life-sciences R&D (biotech/pharma, CRO , or research tech), including end-to-end ownership of a complex product… more
    Genentech (09/06/25)
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  • Clinical Data Strategy & Operations Program Lead…

    AbbVie (North Chicago, IL)
    …Computer Science, or foreign educational equivalent & 5 years of clinical data management experience in a pharmaceutical, CRO or biotech company. Of the ... timelines & quality. + Utilize operational analytics & project management tools to optimize execution of programs & studies,...eCOA, IRT, CDR, SDTM, data visualization tools, risk based management & TMF; & + applying clinical trial processes,… more
    AbbVie (09/05/25)
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  • General Manager

    Charles River Laboratories (Reno, NV)
    …budgets, and operating plans for the site and provides the leadership, management , and strategic focus necessary to deliver business strategy. Essential Duties & ... + At least ten years experience in scientific and management in the life sciences, pharmaceutical, or contract research...River** Charles River is an early-stage contract research organization ( CRO ). We have built upon our foundation of laboratory… more
    Charles River Laboratories (09/04/25)
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  • Medical Director, Clinical Science, Neuroscience…

    Takeda Pharmaceuticals (Cambridge, MA)
    …design and interpretation of clinical studies. Presents study conclusions to Management and determine how individual study results impact the overall compound ... regulatory interactions and future development plans, interacting with upper management of potential partner/acquisition companies during DD visits and alliance… more
    Takeda Pharmaceuticals (09/03/25)
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  • Post-Doctoral Regulatory Affairs Fellow - Product…

    Boehringer Ingelheim (Ridgefield, CT)
    …US RA contributions to all local and global project related documentation such as management summaries, TALC / HPSC / DC pre-reads, are clear, complete and accurate, ... projects and Product Maintenance Optimization strategies, seeking US project team/ management alignment as appropriate. + Assess opportunities for expedited US… more
    Boehringer Ingelheim (08/30/25)
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