• Senior Principal Responsible AI Research

    Autodesk (Boston, MA)
    … directions that align with Autodesk's commitment to safe and responsible AI development **Minimum Qualifications** + PhD in Computer Science, AI/ML, or a ... **Job Requisition ID #** 25WD90901 **Position Overview** As a Responsible AI Research Scientist at Autodesk Research , you will be at the forefront of developing… more
    Autodesk (08/21/25)
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  • Research Scientist - ICH Guidelines

    ThermoFisher Scientific (Boston, MA)
    …to achieve individual career goals while taking science a step beyond through research , development and delivery of life-changing therapies. With clinical trials ... conducted in 100+ countries and ongoing development of novel frameworks for clinical research ...including method SOP, study protocol, technical report, and other regulatory agency facing documents + Be a key Subject… more
    ThermoFisher Scientific (08/29/25)
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  • Senior Responsible AI Research

    Autodesk (Boston, MA)
    **Job Requisition ID #** 25WD86757 **Position Overview** As a Senior Responsible AI Research Scientist-Manager at Autodesk Research , you will be at the forefront ... a key member of the AI Lab in Autodesk Research , you will leverage your expertise in responsible, safe,...align with Autodesk's commitment to safe and responsible AI development + Interest & ability to grow and manage… more
    Autodesk (09/16/25)
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  • Senior Principal Research Scientist, Method…

    AbbVie (Cambridge, MA)
    …and pharmacogenomics. The GRC collaborates across R&D, supporting both discovery research and clinical development , while integrating with process sciences, ... AI/ML algorithms tailored to tackling complex problems across the drug development pipeline, including target discovery, translational research , biomarker … more
    AbbVie (09/24/25)
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  • Clinical Development Program Lead,…

    Bristol Myers Squibb (Cambridge, MA)
    …Stakeholder Engagement and Communication + Will work closely with colleagues in BMS Research , Development , Regulatory , Medical, Commercial and other key ... the field + Partner and interact with colleagues from Research and Early Development who design and...greater than 10 years of extensive clinical trial, drug development , and regulatory experience, in addition to… more
    Bristol Myers Squibb (08/20/25)
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  • Senior Director, Global Development Lead,…

    Pfizer (Cambridge, MA)
    …indications. Typically, work on two to three clinical programs and support the development and provide consultation regarding multiple research projects. + Work ... on all Pfizer Oncology first-in-human clinical trials with input from Oncology Research Unit, Oncology Regulatory Strategy, Clinical Pharmacology and Precision… more
    Pfizer (09/25/25)
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  • Principal Medical Director, Product…

    Genentech (Boston, MA)
    …Medical Director will have strong collaboration with cross-functional teams, including clinical research , regulatory affairs, and product development , to ... Clinical Development Plan (CDP) Strategy & Planning, CDP Execution, Regulatory Activities, and Cross-Functional Team Leadership. + You will mentor other… more
    Genentech (09/12/25)
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  • Global Head, BioAnalytics, CMC Development

    Sanofi Group (Framingham, MA)
    …and with other Sanofi functions (eg, Research , Quality Assurance, Regulatory Affairs, Manufacturing & Supply, Business Development ). **Scope of the ... Experience in transferring analytical methods to commercial QC. Ensure compliance with regulatory standards. + **Drug Development :** Development of products… more
    Sanofi Group (09/20/25)
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  • Senior Principal Scientist, Development

    Bristol Myers Squibb (Cambridge, MA)
    …or related fields, and 8+ or more years of relevant drug discovery and development experience within the pharmaceutical research plus 2+ years of leadership ... multidisciplinary project teams, including developing ADME strategies and implementing drug development plans. + Understanding of regulatory requirements in the… more
    Bristol Myers Squibb (09/25/25)
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  • Director, Early Clinical Development

    Bristol Myers Squibb (Cambridge, MA)
    …support development + Serving as principal functional author for Regulatory submission, study reports, and publications + Provides oversight and medical ... & Strategy** + Designs and develops clinical studies and research plans in support of asset strategy with the...ongoing review of the literature + Keeps abreast of development and regulatory issues related to other… more
    Bristol Myers Squibb (08/12/25)
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