• Research Associate at the CTSA

    University of Pennsylvania (Philadelphia, PA)
    …Army National Guard. The successful applicant will have an opportunity to conduct clinical trials while collecting and analyzing valuable data in a cutting-edge ... of Medicine at the University of Pennsylvania seeks candidates for a Research Associate position in the Academic Support Staff. This appointment will be initially… more
    University of Pennsylvania (12/01/25)
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  • Medical Records Associate

    Ortho Sport and Spine Physicians (Atlanta, GA)
    SUMMARY: The Medical Records Associate is responsible for managing the medical records of patients. This includes scanning documents into the system, as well as, ... retrieving and providing documents upon request. DUTIES: * Data entry (keyboard or scan) and retrieval of medical...* Other duties as assigned REQUIREMENTS: * Strong time management and organizational skills, with attention to detail. *… more
    Ortho Sport and Spine Physicians (11/07/25)
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  • Regulatory Affairs Associate Director, IVD

    GRAIL (Albany, NY)
    …and we are using the power of next-generation sequencing (NGS), population-scale clinical studies, and state-of-the-art computer science and data science to ... + MS or PhD with 10+ years of experience in regulatory, development, clinical affairs, quality, or program management within the IVD, medical device,… more
    GRAIL (12/03/25)
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  • Materials & Logistics Associate - Mt. Holly…

    Virtua Health (Mount Holly, NC)
    …materials management logistics, inventory management , and supply channel management to clinical departments. Adheres to inventory control procedures for ... Services to include shipments, receiving, distribution, inventory, and materials management . Position Responsibilities: Verify quantity and quality of incoming… more
    Virtua Health (12/18/25)
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  • Associate Director, Cell Therapy…

    Bristol Myers Squibb (Summit, NJ)
    …in line with key business milestones & budget. + Utilize standard project management tools and Scrum methodology for tracking and status reporting. + Support ... GMP Manufacturing Operations, Manufacturing Science & Technology, Project & Program management , Quality Assurance / Quality Control Operations and related functions.… more
    Bristol Myers Squibb (12/18/25)
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  • Senior Quality Assurance Associate

    Actalent (Bothell, WA)
    …approve executed test results, perform review tasks in the laboratory information management system to issue Certificates of Analysis (COAs) as applicable. - Provide ... Qualification and Validation activities by providing quality review of associated protocols, data and reports. - Perform internal audits (as applicable). - Support… more
    Actalent (12/10/25)
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  • Associate Director, Scientific Training…

    Takeda Pharmaceuticals (Boston, MA)
    …Takeda Oncology marketed and pipeline products, relevant disease states, and competitor data + Ensure strategic collaboration with regions and countries to better ... fluency with, Takeda Oncology products, respective disease states, and competitor data aligned with product scientific platforms + Develop and execute GMAO… more
    Takeda Pharmaceuticals (12/05/25)
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  • Associate Director, Global Publications

    CSL Behring (King Of Prussia, PA)
    …and compliant scientific publications that advance medical knowledge, support data dissemination, and strengthen CSL Behring's leadership in biotechnology. This ... Publications Director, you will partner with Medical Affairs leaders, Compliance, Clinical , HEOR, and other functions to build efficient processes, trackers, SOPs,… more
    CSL Behring (11/19/25)
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  • Postdoctoral Scholar - Research Associate

    University of Southern California (Los Angeles, CA)
    …research presentations at national conferences. The role will also involve project management , including managing data analyses and manuscript writing. There ... and design phases including curriculum design, prototyping, interview protocols, data collection, data analysis, manuscript writing, and...will be some management tasks that require working with the grants administration… more
    University of Southern California (11/19/25)
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  • Sr. Associate Scientist

    Pfizer (Pearl River, NY)
    …independently to analyze, interpret and summarize experimental data . + Regularly present data and progress to colleagues and senior management . + Maintain a ... in the discovery sciences, ensuring drug safety and efficacy or supporting clinical trials, you will apply cutting edge design and process development capabilities… more
    Pfizer (12/13/25)
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