• Senior Scientific Manager , Medical Affairs

    AbbVie (Mettawa, IL)
    …ability to lead in a global matrixed environment. + Basic knowledge of clinical trial design, results and methodology, regulatory and compliance requirements ... up-to-date therapeutic expertise necessary to serve as a scientific, medical, and clinical partner to field medical teams/affiliates, TA teams, brand teams and R&D… more
    AbbVie (08/19/25)
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  • Research Admin Specialist II- CTMS, US Remote

    Huron Consulting Group (Van Buren, AR)
    …You'll have the opportunity to expand upon your working knowledge and experience with clinical trial regulation, and to develop strong skills in the variety of ... and visit assignments in accordance with Huron and industry standards in Clinical Trial Management Systems ("CTMS"). + Financial console build including… more
    Huron Consulting Group (08/08/25)
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  • Manager , Regulatory Affairs

    Gilead Sciences, Inc. (Foster City, CA)
    …which may include safety reports, amendments, supplements and license renewals to clinical trial applications (eg IND, CTAs), and marketing authorizations), ... to moderately complex programs/projects. + Responsible under guidance of immediate manager for own self-development and acquisition of required regulatory skills and… more
    Gilead Sciences, Inc. (09/06/25)
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  • In-House CRA

    IQVIA (Washington, DC)
    …Research Associate will be a critical team member reporting directly to the Director of Clinical Affairs, to support clinical trial operations for the firm's ... pharmaceutics or a related scientific discipline** **2+ years of clinical trial experience. Monitoring experience preferred.** **Comprehensive knowledge/… more
    IQVIA (09/10/25)
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  • Senior Director, Immunology and Neuroscience,…

    Bristol Myers Squibb (Madison, NJ)
    …to address key data gaps + Coach a team of MEG Leads, inclusive of Clinical Scientists and Clinical Trial Physicians, in successful oversight of Medical ... & Experience** + MD preferred (or x-US equivalent) + 5+ years required clinical trial experience in pharmaceutical industry setting (eg, Clinical more
    Bristol Myers Squibb (09/04/25)
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  • Social Worker- MHRRTP (Transitional Residence…

    Veterans Affairs, Veterans Health Administration (Anchorage, AK)
    …Treatment Programs (MHRRTP) where the social worker is assigned. Provides clinical services, individual and group treatment, and makes appropriate referrals both ... in written and spoken English. You may be required to serve a trial period. Subject to background/security investigation. Selected applicants will be required to… more
    Veterans Affairs, Veterans Health Administration (09/11/25)
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  • Healthcare Engineer (Project Manager )

    Veterans Affairs, Veterans Health Administration (Kansas City, MO)
    …in written and spoken English. You may be required to serve a trial period. Subject to background/security investigation. Selected applicants will be required to ... programs. (c) Ability to understand the operational professional engineering needs of clinical services in the healthcare system. (d) Ability to prepare material on… more
    Veterans Affairs, Veterans Health Administration (09/06/25)
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  • Senior Project Manager , Cell Therapy…

    Bristol Myers Squibb (Princeton, NJ)
    …across a matrix. + Experience with drug development, commercialization, and healthcare, clinical trial management a plus. \#LI-Hybrid If you come across ... unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency,… more
    Bristol Myers Squibb (08/28/25)
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  • Principal CoreValve Therapy Development Specialist

    Medtronic (Orlando, FL)
    …RESPONSIBILITIES:** The following responsibilities are to be performed as appropriate in clinical trial case support and/or case support following commercial ... wave forms, and ancillary procedural solutions + Knowledge of Clinical trial protocols and CoreValve and other...information regarding product price or account activity to District Manager and other appropriate company personnel + Ensure a… more
    Medtronic (09/11/25)
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  • Research Coordinator Lead

    University of Washington (Seattle, WA)
    …enrollment, treatment, and long term follow up. Catalog and document all designated clinical trial protocols currently accruing at UW-affiliated sites, and to ... periodic auditing of study documentation and representing the CRC Manager in their absence on committees or project audits...update clinicians about other new/available clinical trial protocols. Abstract data from … more
    University of Washington (09/06/25)
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