• Director , Toxicology

    Editas Medicine (Cambridge, MA)
    …therapies to patients with genetic disorders. Characterizing Your Impact: As the Director , Toxicology you will: + Develop phase-appropriate nonclinical safety ... leadership role, you will serve as the Head of Toxicology within Editas and be responsible for overseeing all...the design and oversee execution of GLP and non-GLP toxicology studies to support regulatory submissions and interactions with… more
    Editas Medicine (10/12/25)
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  • Associate Director , Non-Clinical Research

    Rhythm Pharmaceuticals (Boston, MA)
    …together. Opportunity Overview Rhythm Pharmaceuticals is seeking an Associate Director , Non-Clinical Research with demonstrable experience and expertise in small ... overall company strategy. This role will report into the Sr. Director , Non-Clinical Development. Responsibilities and Duties + Support/lead Rhythm's non-clinical… more
    Rhythm Pharmaceuticals (08/20/25)
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  • Senior Recreational Water Quality Scientist

    State of Massachusetts (Boston, MA)
    …coordinator of the Bathing Beaches Project in the Division of Environmental Toxicology , Hazard Assessment and Prevention. Directs other professional staff in the ... coordinator of the Bathing Beaches Project in the Division of Environmental Toxicology , Hazard Assessment and Prevention. * Supervise Bathing Beaches Project staff… more
    State of Massachusetts (09/13/25)
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  • Director , Quantitative Clinical…

    Takeda Pharmaceuticals (Cambridge, MA)
    …scientific and operational sub-teams. + Collaborates cross-functionally with discovery, toxicology , and other QPTS functions to ensure that preclinical findings ... for drug development, such as statistics, drug metabolism, pharmacology, toxicology , bioanalysis, and pharmaceutical science. + Ability to evaluate Benefit-Risk… more
    Takeda Pharmaceuticals (09/09/25)
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  • Associate Director , In Vivo Digital…

    Takeda Pharmaceuticals (Boston, MA)
    …application is true to the best of my knowledge. **Job Description** **Associate Director , In Vivo Digital Portfolio & Data Stewardship** **About the Role** We are ... seeking an experienced **Associate Director of In Vivo Digital Portfolio & Data Stewardship**...and end-to-end in vivo/ex vivo workflows. + Exposure to **safety/ toxicology and pathology data workflows** to support Safety (NCSP)… more
    Takeda Pharmaceuticals (10/11/25)
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  • Regulatory Affairs Director (US)

    Chemours (Boston, MA)
    …and more modern living depend on Chemours chemistry. Chemours is seeking a ** Director of Regulatory Advocacy** to join our growing Government Affairs team! This ... of Excellence, Corporate Sustainability, Corporate Product Regulatory Compliance, Corporate Toxicology and Risk Assessment, Finance, and Communications, among others,… more
    Chemours (08/14/25)
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  • Director , Small Molecule In Vitro…

    Takeda Pharmaceuticals (Boston, MA)
    …to the best of my knowledge. **Job Description** **_Objective / Purpose:_** The Director , Small Molecule In Vitro Pharmacology (IVP) plays a pivotal role in small ... by aligning with key stakeholders, including internal biology, pharmacokinetics, toxicology , computational sciences, and structural biology/protein chemistry teams. Collaborate… more
    Takeda Pharmaceuticals (07/26/25)
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  • Scientific Director - ADME Project…

    Lilly (Boston, MA)
    …with cross-functional colleagues in both Discovery and Development (eg. Toxicology , Pharmacology, Chemistry, Clinical PK/PD, Clinical Pharmacology, Regulatory, and ... Medical) to assess drugability and optimize ADME properties to deliver drug candidates to the clinic, as well as to design and support nonclinical and clinical studies, supporting global registration packages. * Lead R&D initiatives to grow and develop… more
    Lilly (10/10/25)
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  • Director , Pharmaceutical Sciences Program…

    Takeda Pharmaceuticals (Boston, MA)
    …and/or regulatory affairs. Advanced understanding in DMPK, Pharmacology and Toxicology . + Extensive knowledge of current Good Manufacturing Practices (cGMP), ... ICH Guidelines, other pertinent national regulations, compendial requirements and communicating with regulatory agencies. + Must have experience in global regulatory submission requirements and processes. **Program Leadership Skills/Competencies:** Experience… more
    Takeda Pharmaceuticals (09/25/25)
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  • Associate Director , Chemical Stewardship

    Bristol Myers Squibb (Devens, MA)
    …risk. **Qualifications & Experience** + Bachelors degree in chemistry, toxicology , product stewardship or related discipline required. Advanced degree preferred. ... + 10+ years regulatory experience in chemicals (experience with complex portfolios and multinational organizations is highly valued). In-depth knowledge of global chemical regulations and registrations processes applicable for the pharmaceutical industry. +… more
    Bristol Myers Squibb (09/18/25)
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