• Director of Investigations - Americas

    CBRE (Los Angeles, CA)
    …of Investigations - Americas Job ID 219422 Posted 20-May-2025 Service line Corporate Segment Role type Full-time Areas of Interest Legal Location(s) Los Angeles ... ethical excellence, accountability, and continuous development. - Oversee complex internal investigations into allegations of serious misconduct including fraud,… more
    CBRE (05/22/25)
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  • Medical Science Liaison/ Sr. MSL/ Principal MSL

    Medexus Pharma (Remote, OR)
    …centers of excellence engagement plans. + Facilitate the submission of investigator -initiated trials and collaborative research inquiries, including the provision of ... policies. + Support the creation of Medical Affairs documents in alignment with corporate objectives to include, but not limited to, slide decks, standard response… more
    Medexus Pharma (05/15/25)
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  • Advisor, Clinical Research

    Abbott (Santa Clara, CA)
    …position will be required to execute their job responsibilities within the corporate policies and standard operating procedures. **What You'll Work On** + Design ... clinical trials and studies in collaboration with internal stake holders including clinical project management, clinical operations, biostatistics data management,… more
    Abbott (05/28/25)
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  • Senior Director, Clinical Development - Hematology

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …for one or more clinical trials + Matrix management responsibilities across the internal and external network + Manages Phase 1 - Phase 3 studies (depending ... as needed + Study-specific subject matter expert (ME) for internal audit or Health Authority (HA) questions related to...+ May lead the development and updates of the Investigator 's Brochure (IB): author the clinical section and lead… more
    Daiichi Sankyo Inc. (04/04/25)
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  • Senior Medical Director/Medical Director, Clinical…

    AbbVie (North Chicago, IL)
    …deliverables. Responsible for assessment and reporting of serious adverse events per corporate policy and regulations for those protocols on which assigned. + ... analysis, interpretation, and reporting of scientific content of protocols, Investigator Brochures, Clinical Study reports, regulatory submissions and responses, and… more
    AbbVie (06/07/25)
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  • Medical Director, Clinical Development - Eye Care

    AbbVie (Irvine, CA)
    …deliverables. Responsible for assessment and reporting of serious adverse events per corporate policy and regulations for those protocols on which assigned. + ... analysis, interpretation, and reporting of scientific content of protocols, Investigator Brochures, Clinical Study Reports, regulatory submissions and responses, and… more
    AbbVie (05/30/25)
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  • Grant Writer

    University of Maryland, Baltimore (Baltimore, MD)
    …effort will be devoted to writing and editing large, multi- investigator , multi-site NIH applications./*This is a full-time, regularfully remoteposition. */ ... research and public information materials, including University website. * Performs internal reviews of institutional needs and assess the feasibility of obtaining… more
    University of Maryland, Baltimore (05/29/25)
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  • Director, WW Medical Oncology, GI

    Bristol Myers Squibb (Princeton, NJ)
    …in scientific communication to ensure delivery of key knowledge to the internal stakeholders including local medical market colleagues; ensure global alignment and ... communication efforts to ensure delivery of key knowledge to the internal stakeholders including local medical market colleagues; ensure alignment across global… more
    Bristol Myers Squibb (06/09/25)
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  • Senior Quality Control Analyst

    Glenmark Pharmaceuticals Inc., USA (Monroe, NC)
    …Ensure that the QC Laboratory is in a ready state of compliance for internal and external audits. + Execute technology transfer of analytical methods for new ... CAPA for Lab failures in OOS. + Complete and maintain certified investigator training requirements to ensure SIT representation for identified area(s). + Performing… more
    Glenmark Pharmaceuticals Inc., USA (06/03/25)
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  • Trial Supplies Manager

    System One (Trenton, NJ)
    …to ensure timely delivery of supplies to study participants. * Collaborating with internal and external Customers and Service Providers, including but not limited to ... use of the investigational material supply chain to achieve study and corporate goals. * Identifying and supporting strategies for continuous improvement and… more
    System One (05/30/25)
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