• Associate Director , Biostatistics

    BeOne Medicines (San Mateo, CA)
    …study/project teams supporting hematology studies and interact with Clinical , Regulatory, Statistical Programming, Data Management and other Research ... and implementing the statistical analysis plan (SAP) for the clinical study report (CSR) and other health authority submission...to ensure that the data evaluated are in high quality and satisfy analysis requirements. + Collaborates with the… more
    BeOne Medicines (09/23/25)
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  • Associate Principal Scientist, Device Risk…

    Merck (West Point, PA)
    **Job Description** The Associate Principal Scientist, Device Risk Management Lead, is a crucial member of our team, responsible for spearheading risk management ... oversee device risk management activities to ensure the delivery of high- quality products and efficient manufacturing processes. The role requires extensive… more
    Merck (12/13/25)
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  • Associate Director , Statistics…

    AbbVie (North Chicago, IL)
    …strategies for assigned projects; for the design, analysis, and reporting of clinical and other scientific research programs; for generating scientific evidence to ... data related issues arising in the design, conduct or analysis of clinical trials or other scientific research. Independently select, evaluate and implement… more
    AbbVie (10/10/25)
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  • Associate Director , Global R&D…

    BeOne Medicines (San Mateo, CA)
    **General Description:** This position will be responsible for the management of clinical outsourcing needs in support of BeOne's current and planned clinical ... metrics, and vendor oversight/governance. This position will also be responsible for clinical study budget estimation and budget management during the study life… more
    BeOne Medicines (11/25/25)
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  • Associate Director , Automation…

    Merck (Rahway, NJ)
    …availability of Clinical Supplies and Development Batches to meet Clinical Development Program requirements. + Partners with Quality , Operations, Technology, ... experience. **Required Experience and Skills** : + Strong familiarity with Quality , cGMP, Safety & Environmental Policies and Procedures. + Demonstrated technical… more
    Merck (11/25/25)
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  • Associate Director , Statistics…

    Takeda Pharmaceuticals (Boston, MA)
    …patients with our quantitative skills. We design efficient trials, contribute to clinical development strategies, perform high quality statistical analyses, and ... scientists (from statistics, programming, outcomes research and epidemiology, quantitative clinical pharmacology, digital strategy, library sciences and data architecture/governance)… more
    Takeda Pharmaceuticals (09/20/25)
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  • Associate Director , Planning…

    Merck (West Point, PA)
    …data-driven operations across GMP manufacturing. Based in the Bioprocess and Clinical Manufacturing Technology Department within the Biologics Pilot Plant (BPP) in ... System/Electronic Batch Record) initiatives. This role requires intense collaboration with Quality (QA/QC) and will serve as the primary interface between the… more
    Merck (12/12/25)
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  • Director of Wellness, Quality

    Allegro Management Company Llc (Clayton, MO)
    …expectations. The only thing missing is YOU! The Director of Wellness, Quality and Education is responsible for providing clinical expertise and for ... excellent resident services, high occupancy, and high resident and associate satisfaction are always the goal of the Company....+ Analyzes resident and clinical reports with Director of Wellness, Quality and Education and… more
    Allegro Management Company Llc (09/28/25)
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  • Associate Director , Statistics

    Takeda Pharmaceuticals (Boston, MA)
    …patients with our quantitative skills. We design efficient trials, contribute to clinical development strategies, perform high quality statistical analyses, and ... for one or more assets at GPT level or specialty area in clinical + Facilitate execution and delivery collaboration cross functionally in Global Project Teams… more
    Takeda Pharmaceuticals (12/11/25)
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  • Regulatory Affairs Associate

    GRAIL (Concord, NH)
    …+ **Experience** + Minimum of 10 years of experience in regulatory, development, clinical affairs, quality , or program management within the IVD, medical device, ... 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 overcome… more
    GRAIL (12/03/25)
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