• Senior Manager, Global Regulatory Labeling…

    Takeda Pharmaceuticals (Boston, MA)
    …and executes a labeling implementation plan to incorporate new scientific, safety and clinical data , as well as Health Authority responses / feedback into ... bring life-changing therapies to patients worldwide. Join Takeda as Senior Manager, Global Regulatory Labeling Strategy where you will be responsible for the… more
    Takeda Pharmaceuticals (12/11/25)
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  • Director I, Aesthetics Clinical Development

    AbbVie (Irvine, CA)
    …cross-functional teams to generate, deliver and interpret high quality research and clinical data supporting aesthetic indications and overall asset program ... required, consistent with corporate policies. + Ensures adherence to Good Clinical Practices, pharmacovigilance standards , standard operating procedures and to… more
    AbbVie (12/09/25)
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  • Associate Director, Device Clinical

    Takeda Pharmaceuticals (Lexington, MA)
    …in the Drug Product and Device Development (DPDD) group provides strategic clinical leadership for global device and combination product development programs. ... clinical outcomes that exceed quality benchmarks and regulatory standards . **Core Responsibilities:** **Device Clinical Strategy &... functions and device development teams + Serve as clinical liaison to Global Device Team, including… more
    Takeda Pharmaceuticals (12/04/25)
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  • Supervisor, Clinical Services

    ICON Clinical Research (San Antonio, TX)
    …and IRB processes + Strong skills in protocol review, eligibility assessment, medical/ clinical documentation, and source data verification + Excellent verbal and ... Supervisor, Clinical Services (Early Phase Research- Screening)- ICON San...requirements in accordance with study protocols, SOP's, and ICH-GCP standards ._ Location: 100% on site San Antonio TX What… more
    ICON Clinical Research (10/15/25)
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  • Clinical Research Nurse I (PRN)

    ICON Clinical Research (Lenexa, KS)
    …Nurse at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data , and contributing to the advancement of ... monitor patient reactions during clinical trials. + Collect and manage clinical trial data , ensuring accuracy and completeness. + Provide patient education… more
    ICON Clinical Research (12/16/25)
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  • Senior Principal Scientist, Clinical

    Merck (San Francisco, CA)
    Clinical Judgment, Clinical Medicine, Clinical Research Management, Clinical Trial Development, Clinical Trials, Data Analysis, Drug Development, ... **Job Description** Our Clinical and Pharmacovigilance teams manage studies to provide...teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new drugs,… more
    Merck (12/02/25)
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  • Assistant Clinical Research Coordinator…

    Stanford University (Stanford, CA)
    …causes. The ACRC will perform administrative support duties related to the collection of clinical data and/or the coordination of clinical studies for lung ... Assistant Clinical Research Coordinator (Hybrid Opportunity) **School of Medicine,...records and/or perform telephone or in-person interviews to gather data , as needed. + Administer standard study questionnaires and… more
    Stanford University (12/05/25)
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  • Clinical Research Coordinator

    University Of Vermont (Burlington, VT)
    …Perform data entry, QA/QC and data analysis, maintaining the highest standards of Good Clinical Practice. Prepare data and safety reports and ... Position Details Advertising/Posting Title Clinical Research Coordinator Posting Summary Provide clinical...creating an inclusive environment that embraces intellectual diversity and global perspectives. We seek to prepare students to be… more
    University Of Vermont (12/15/25)
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  • Clinical Research Coordinator

    Actalent (Lima, OH)
    …strong attention to detail. + Strong computer skills with demonstrated abilities using clinical trials databases, IVR systems, electronic data capture, MS Word, ... office flow with Investigator and site staff. + Record data legibly and enter in real-time on paper or...and research personnel. The work requires adherence to regulatory standards and involves collaboration with clinical staff… more
    Actalent (12/13/25)
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  • Clinical Research Coordinator Associate

    Stanford University (Stanford, CA)
    clinical practice guidelines as well as collecting, recording and maintaining complete data files using good clinical practice in accordance with HIPAA ... of study specimens and processing. + Collect and manage patient and laboratory data for clinical research projects. Manage research project databases, develop… more
    Stanford University (12/08/25)
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