• Supervisor

    Charles River Laboratories (Boston, MA)
    …staff in the following: cage changing, microisolator cage changing techniques, room sanitation, autoclave operation, cagewash operations, waste disposal and other ... as needed. + Responsible for developing and maintaining animal records including, room logs, health reports, cage card labels, autoclave records, cagewash records,… more
    Charles River Laboratories (09/01/25)
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  • Director, Comparator Sourcing

    BeOne Medicines (Emeryville, CA)
    …12+ years progressive experience in Supply Chain preferably within the biotech, pharmaceutical, CRO , industry with 5+ years in comparator sourcing + 5+ years of ... people leadership and development experience **Computer Skills :** Efficient in Microsoft Word, Excel, and Outlook All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender… more
    BeOne Medicines (09/01/25)
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  • Traveling Reset Specialist - Coborns

    Acosta Group (Fargo, ND)
    **Traveling Reset Specialist - Coborns** **General Information** **Company:** CRO -US **Location:** FARGO, North Dakota, 58103 **Ref #:** 97660 **Function:** ... Merchandising **Employment Duration:** Full-time **Description and Requirements** **CROSSMARK** is seeking an energetic, motivated individual to join our growing team. As part of our family, you'll support Coborn's, a reputable employee-owned grocery chain.… more
    Acosta Group (08/31/25)
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  • Manager, Strategic Sourcing, R&D

    Sumitomo Pharma (Bismarck, ND)
    …that are in accordance with corporate ethics, financial policy, and internal control requirements + Pursue ongoing development of relevant skills, including learning ... range of service categories in the R&D space, preferably with CRO and ancillary vendor contract negotiation and oversight responsibilities. Pharmaceutical,… more
    Sumitomo Pharma (08/30/25)
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  • Senior Principal Scientist, Analytical Chemistry…

    Lilly (Indianapolis, IN)
    …will be tasked with developing and implementing robust analytical methods and control strategies to enable clinical trial material delivery and build process ... understanding. **Responsibilities:** + Collaborate with project teams to develop robust control strategies for drug substances and drug products, enable clinical… more
    Lilly (08/30/25)
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  • Senior Director, Clinical Development, Breast…

    BeOne Medicines (Emeryville, CA)
    …scientific expertise for selection of investigator and vendors + Train BeOne colleagues, CRO staff, and study site staff on the therapeutic area, molecule, and/or ... clinical protocol + Provide scientific and medical support throughout conduct of a clinical trial; respond to clinical questions from sites, IRBs/IECs, Health Authorities, and CROs + Review, query, and analyze clinical trial data + Interpret, and present… more
    BeOne Medicines (08/30/25)
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  • Risk Management - Control Manager - Vice…

    JPMorgan Chase (Columbus, OH)
    …as required (CCOR, Legal, Central Program Team). + Support meeting administration (eg, Control Sub-Committees and CRO Control Updates), including producing ... As a Risk Control Manager Vice President, you will play a...play a crucial role in overseeing and executing the control environment for Asset and Wealth Management Risk. You… more
    JPMorgan Chase (08/30/25)
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  • Statistical Science Lead, Safety Statistician

    Astellas Pharma (Northbrook, IL)
    …MS) of experience in applying statistical methods in biomedical research, Pharma, CRO , Academia or Healthcare industry or in providing statistical direction in these ... areas + Advanced and broad knowledge of statistical methods, along with understanding of industry practices related to the statistical analysis of clinical and biomarker data + Knowledge and skills in SAS required, knowledge of R preferred. + In-depth… more
    Astellas Pharma (08/30/25)
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  • Post-Doctoral Regulatory Affairs Fellow - Product…

    Boehringer Ingelheim (Ridgefield, CT)
    …(eg Due Diligence) and contribute to assessment reports. For projects with a CRO or licensing partner, provide and implement US RA strategic and operational ... perspectives/tasks, as appropriate. + Health Authority Interactions/Submissions: + Responsible for all FDA interactions on assigned projects/products, including formal meetings, FDA review of registration packages, and labeling negotiations. + Establish and… more
    Boehringer Ingelheim (08/30/25)
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  • Highly Distinguished/ Distinguished Research…

    Boehringer Ingelheim (Ridgefield, CT)
    …investigative study work packages, developing study designs and their placement (internal, CRO ) and execution * Capable of independently serving as broad subject ... matter expert to global senior leadership and R&D governance committees; It is expected that the incumbent will have an unimpeachable record of high level impact on a drug discovery and development portfolio. * Maintain and expand an international reputation… more
    Boehringer Ingelheim (08/30/25)
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