• Associate Director , Clinical Program…

    Takeda Pharmaceuticals (Boston, MA)
    …best of my knowledge. **Job Description** **About the role:** Associate Director , Clinical Program Quality Investigations is responsible for ensuring the compliance ... right stakeholders are engaged in impact assessment, root cause analysis and CAPA development . + Oversee the Serious Breach Reporting Service and ensure that the… more
    Takeda Pharmaceuticals (07/16/25)
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  • Director , Clinical Operations

    Bausch + Lomb (Boston, MA)
    …over our 170-year history. We have a significant global research, development , manufacturing and commercial footprint of approximately 13,000 employees and a ... areas of Responsibility** **:** Clinical Operations: + Manage and/or oversee the development process for critical study documents (eg, protocol, amendments, IB, ICF,… more
    Bausch + Lomb (06/07/25)
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  • Associate Director - Life Sciences Advisory…

    Guidehouse (Boston, MA)
    …for specialty medications (eg, high cost, biologics, CAR-T, REMs, drug-device combinations), Organizational design and change management, and Primary research. + ... You Will Do** **:** The Patient Services team provides program design , implementation, and monitoring services to pharmaceutical, biotechnology, and medical device,… more
    Guidehouse (08/18/25)
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  • Strategic Partner Director , National TPA…

    Manulife (MA)
    …seeking a dynamic and strategic leader to join our team as Strategic Partner Director , National TPA Channel. In this role, you will strengthen partnerships with key ... sales strategy to grow business with strategic TPA partners. + Partnership Development : Collaborate with TPA Channel Directors to build joint business plans that… more
    Manulife (08/23/25)
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  • Associate Director , Clinical and Safety…

    Takeda Pharmaceuticals (Boston, MA)
    …best of my knowledge. **Job Description** **About the role:** The Associate Director , Clinical and Safety Quality Compliance is responsible for ensuring the quality ... of new and revised processes across CPMQ. + Contributing to the design , implementation and advancement of the Clinical and Safety Quality Compliance strategy,… more
    Takeda Pharmaceuticals (07/25/25)
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  • Director of Labor Relations

    Clean Harbors (Norwell, MA)
    The ** Director , Labor Relations** is responsible for oversight and management of all aspects of the labor relations portfolios within the organization (US and ... labor contract administration. Will formulate labor and employment policy development and training. Negotiates collective bargaining agreements, resolves disputes,… more
    Clean Harbors (07/16/25)
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  • Regional Sales Director - Southern…

    Trustmark (Boston, MA)
    …to our colleagues, clients and communities. **About the role** Regional Sales Director - Southern California Trustmark Voluntary Benefits is a division of Trustmark ... the sales process and contributing to sales planning, forecasting and product development . **Key Accountabilities** + Achieve annual new business sales, net growth &… more
    Trustmark (06/21/25)
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  • AI Governance Associate Director

    Wolters Kluwer (Waltham, MA)
    …8 days per month at an approved Wolters Kluwer location._** The **AI Governance Associate Director ** will serve as a key leader in the evolution and execution of the ... their roles, responsibilities, and the value of compliant and responsible AI development . This includes both the initial rollout and ongoing updates as the… more
    Wolters Kluwer (06/20/25)
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  • Director , Operations

    Charles River Laboratories (Shrewsbury, MA)
    …75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, ... revenue targets. Collaborate with clients and scientific staff for effective study design , problem solving, and delivery of high-quality study data. Foster a culture… more
    Charles River Laboratories (07/08/25)
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  • Director , Pharmacometrician

    Pfizer (Cambridge, MA)
    …coupled with strong interpersonal abilities. + Deep understanding of clinical trial design , principles of clinical development , and related disciplines. + Proven ... with 4+ years of experience. + A profound understanding of clinical trial design , principles of clinical development , and related disciplines such as clinical… more
    Pfizer (08/22/25)
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