• Senior Scientist, I, siRNA in vitro Biology

    AbbVie (Cambridge, MA)
    …and/or as a primary inventor of patents. Qualifications + BS, MS, or PhD in Cell Biology, Molecular Biology, Biochemistry, or related field with typically 10+ ... (BS), 8+ (MS), or 0+ ( PhD ) years of relevant experience. + Extensive hands-on experience...skills, including experience contributing to technical reports, publications, or regulatory documentation. If you are passionate about advancing RNA-based… more
    AbbVie (08/15/25)
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  • Staff Machine Learning Engineer - (Platform)

    Coinbase (Boston, MA)
    …for in you: * 8+ years of industry experience in Machine Learning (or PhD +5) * Prior experience working with Payment Risk/Credit Risk/Account Take Over models. * MS ... in Machine Learning, Computer Science, other technical field ( PhD preferred) * Strong developer experience with ability to leverage auto-code generation techniques… more
    Coinbase (08/09/25)
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  • Research Fellow in Global Mental Health…

    Harvard University (Cambridge, MA)
    …task-sharing for scale-up of proven interventions. We welcome applications from recent PhD graduates who are interested in these or related fields, particularly ... proposals to fund the research; secure and maintain IRB and regulatory approvals; conduct analysis, publish findings, and disseminate research findings through… more
    Harvard University (08/07/25)
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  • Senior Distinguished Scientist, Immunoscience…

    Sanofi Group (Cambridge, MA)
    …therapies into frontier indications with the explicit goal of future regulatory approval, by applying strong mechanistic rationale, translational insight, and ... strategic prioritization + Drive entry into emerging scientific areas by exploring under-recognized immune mechanisms, novel biology, and cross-disease pathway insights that broaden the scientific reach of the pipeline + Design and oversee target validation… more
    Sanofi Group (07/31/25)
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  • Imaging Technology Lead

    GE HealthCare (Boston, MA)
    …trials, at the heart of which are Imaging Technology Leads (typically PhD /MD/PGDip/MSc level) with subject matter expertise in imaging science and technology. In ... + Author and review imaging sections of trial-facing and regulatory documents + Collaborate with R&D Digital colleagues in...in Clinical Ultrasound (UK - or international equivalent) and/or PhD or MD in a relevant science discipline such… more
    GE HealthCare (07/30/25)
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  • Director, Translational Medicine, Immunology (MD…

    Otsuka America Pharmaceutical Inc. (Boston, MA)
    …and execution. The ideal candidate is an experienced physician-scientist (MD, MD/ PhD ) with a strong background in early clinical development, biomarkers, and ... vivo systems to support program hypotheses and biomarker discovery. + Support regulatory filings including INDs, IBs, and CTAs, with specific responsibility for… more
    Otsuka America Pharmaceutical Inc. (07/09/25)
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  • Senior Antenna Design Engineer

    General Atomics (Boston, MA)
    …**Job Qualifications:** + Typically requires a bachelors degree, masters degree or PhD in engineering or a related technical discipline from an accredited ... masters degree, or seven or more years with a PhD . May substitute equivalent engineering experience in lieu of...as MATLAB, ADS, HFSS, and/or CST + Knowledge of regulatory requirements (FCC, etc.) + Previous experience working with… more
    General Atomics (06/29/25)
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  • Senior Manager, Statistics

    Takeda Pharmaceuticals (Boston, MA)
    …support data-driven decisions in clinical development + Participate in preparation of regulatory submissions and responses to regulatory agencies. + Contribute ... industry standards applicable to the design, analysis of clinical trials and regulatory submissions. + Strong statistical programming skills (SAS and R) + Excellent… more
    Takeda Pharmaceuticals (08/22/25)
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  • IT Auditor I

    Fresenius Medical Center (Waltham, MA)
    …Provides guidance, support and subject matter expertise to the FMCNA IT Regulatory function, who, in turn, works directly with IT management in documenting/testing ... year. + Facilitate regular meetings with the FMCNA IT Regulatory function and IT management to plan the documentation...a Master's degree with 3 years' experience; or a PhD without experience; or equivalent directly related work experience.… more
    Fresenius Medical Center (08/16/25)
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  • Associate Director, Quantitative Pharmacology,…

    Otsuka America Pharmaceutical Inc. (Boston, MA)
    …**pharmacometrics** activities related to pre-IND, IND, phase1-3, PK, PK/PD and regulatory submissions. You will conduct analysis, execution and reporting of ... + Author **pharmacometrics sections** of clinical pharmacology documents for regulatory filings including annual reports, investigator's brochure, IND/NDA applications… more
    Otsuka America Pharmaceutical Inc. (08/16/25)
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