• Associate Director

    Sumitomo Pharma (Providence, RI)
    …currently seeking a dynamic, highly motivated, and experienced individual for the position of ** Associate Director , Regulatory Affairs ** . The ... Associate Director is part of the Global Regulatory Affairs (GRA) team based in the US. He/she is expected to provide regulatory support from proof of… more
    Sumitomo Pharma (11/21/24)
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  • Associate Director , Global…

    Takeda Pharmaceuticals (Boston, MA)
    …order to bring life-changing therapies to patients worldwide. As an Associate Director , Global Regulatory Affairs Marketed Products you will define, ... and influencing the field as applicable. **How you will contribute:** + The Associate Director will be responsible for increasingly complex or multiple projects.… more
    Takeda Pharmaceuticals (12/07/24)
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  • Associate Director , Field Medical…

    Sumitomo Pharma (Providence, RI)
    …. **Job Overview** Associate Director , Field Medical and Scientific Affairs ... summarizes, and disseminates key insights obtained from the RDs to the Medical Affairs and other internal stakeholders in a timely manner. + Participate in the… more
    Sumitomo Pharma (12/14/24)
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  • Director , Residence Life, Division…

    Boston University (Boston, MA)
    …Oversight: Lead the central administrative office team and provide supervision to the Senior Associate Director of Residence Life, Associate Director of ... As a pivotal leader within the Division of Student Affairs , the Director of Residence Life reports...Residence Life for Administration, Associate Director of Residence Life for Student & Staff Development,… more
    Boston University (11/29/24)
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  • Associate Director , Global…

    Takeda Pharmaceuticals (Providence, RI)
    …company that will inspire you and empower you to shine? Join us as an Associate Director , Global Regulatory Project Management and Strategic Planning - ... Neuroscience TAU within our Global Regulatory Affairs organization, based remotely. + Partners with the Global Regulatory Lead (GRL) on Global Regulatory more
    Takeda Pharmaceuticals (01/19/25)
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  • Associate Director , Global…

    Takeda Pharmaceuticals (Boston, MA)
    …in order to bring life-changing therapies to patients worldwide. Join Takeda as an Associate Director , Global Regulatory Lead, GI & Inflammation where you ... field as applicable. **How you will contribute:** + The Associate Director will be responsible for complex...regulatory strategy such as understanding broad concepts within regulatory affairs and implications across the organization… more
    Takeda Pharmaceuticals (12/21/24)
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  • Associate Director , Global…

    Takeda Pharmaceuticals (Boston, MA)
    …primary liaison to the US FDA and provides support for regional and local regulatory affairs teams for interactions with international regulatory Agencies ... interactions/meetings related to assigned programs and supports regional and local regulatory affairs teams with health authority interactions. + Ensures… more
    Takeda Pharmaceuticals (01/18/25)
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  • Associate Medical Director

    Chiesi (Boston, MA)
    …**_Who we are looking for_** **Purpose** The position of Associate Medical Director reports to the Head of Medical Affairs Hematology- Immunology Medical ... Associate Medical Director , Hematology and Immunology...Director and is part of the Global Medical Affairs team supporting the development and implementation of the… more
    Chiesi (12/17/24)
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  • Associate Director Data Analysis…

    Dana-Farber Cancer Institute (Boston, MA)
    The Associate Director , Data Analysis and Management, under the Director and the PI of the Cohort Studies, is responsible for the oversight, management and ... Department of Breast Oncology. The primary focus of the Associate Director , Data Analysis and Management is...academic institution is preferred. + Must have knowledge of regulatory affairs , research ethics and the responsible… more
    Dana-Farber Cancer Institute (11/22/24)
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  • Associate Director , Global Medical…

    Takeda Pharmaceuticals (Boston, MA)
    …true to the best of my knowledge. **Job Description** **Objectives/Purpose** The Associate Director , Global Medical Communications, Immunology is a key strategic ... for assigned assets. In strategic partnership with cross-functional stakeholders, the Associate Director , Global Medical Communications, Immunology will: + Lead… more
    Takeda Pharmaceuticals (11/13/24)
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  • Associate Director , Global Labeling…

    Takeda Pharmaceuticals (Providence, RI)
    …in order to bring life-changing therapies to patients worldwide. Join Takeda as Associate Director , Global Labeling Lead where you will be responsible for ... and assures that Takeda labeling content and processes conform to regulatory requirements. Management of Local Exceptions and LOC Interactions + Manages… more
    Takeda Pharmaceuticals (01/15/25)
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  • Associate Director , Quantitative…

    Takeda Pharmaceuticals (Boston, MA)
    …to bring life-changing therapies to patients worldwide. Join Takeda as an Associate Director , Quantitative Clinical Pharmacology Lead in Cambridge, MA, where ... Drug Safety, Clinical Sciences, Outcomes, Digital Health, Pharmaceutical Sciences/Device, and Global Regulatory Affairs . + Advanced knowledge of regulatory more
    Takeda Pharmaceuticals (01/10/25)
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  • Compliance Operations Lead, Associate

    Takeda Pharmaceuticals (Boston, MA)
    …processes and training and ensure alignment with global processes and regulatory requirements and expectations. + Drive the implementation and change management ... enable execution of CPMQ activities, ensuring alignment with global processes and regulatory requirements. + Create and deliver training solutions to support the… more
    Takeda Pharmaceuticals (12/20/24)
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  • Executive Director - Various Boards Unit

    State of Massachusetts (Boston, MA)
    …misconduct. The Executive Director ("ED") for the Unit reports to the Associate Deputy Commissioner for Policy & Boards ("ADC"). At the direction of the ADC, ... Licensure (DOL), an agency within the Office of Consumer Affairs and Business Regulation (OCABR), protects consumers by making...procedures, and policies that direct the daily licensing and regulatory activities of the boards within the Unit. The… more
    State of Massachusetts (01/17/25)
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  • Contract Center Medical Director /Center…

    CSL Plasma (Warwick, RI)
    …Staff Associates for completion of training and recommendation for certification by Regulatory Affairs . Functionally directs the Center Medical Staff. Provides ... as or delegates to another appropriate physician the duties of "laboratory director ", "technical consultant", or "clinical consultant" as prescribed by the Clinical… more
    CSL Plasma (01/13/25)
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  • Research Contract Associate

    Beth Israel Lahey Health (Boston, MA)
    …a job, you're making a difference in people's lives.** Reporting to the Associate Director , Sponsored Programs Contracting Office (SPC), the Research Contract ... (FFATA) system for subcontract activity on awarded federal grants. (essential)** **Works with Associate Director of SPC, SPC staff and periodically with the… more
    Beth Israel Lahey Health (12/22/24)
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  • Sr. Associate , Internal Audit

    Commonwealth Care Alliance (Boston, MA)
    …duties as assigned. **Secondary Responsibilities** + Contribute towards the overall Department Regulatory Affairs and Compliance infrastructure at CCA. + Promote ... 012100 CCA-Internal Audit **Position Summary** Under direction of the Director of Internal Audit, the primary functions of this position are to: + Contribute towards… more
    Commonwealth Care Alliance (11/26/24)
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  • Internal Audit Associate

    Commonwealth Care Alliance (Boston, MA)
    …duties as assigned. **Secondary Responsibilities** + Contribute towards the overall Department Regulatory Affairs and Compliance infrastructure at CCA. + Promote ... 012100 CCA-Internal Audit **Position Summary:** Under direction of the Director of Internal Audit, the primary functions of this position are to: + Contribute… more
    Commonwealth Care Alliance (11/26/24)
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  • Principal Scientist, Clinical Research, Immunology

    Merck (Boston, MA)
    …+ Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... to pursue and subsequent study design, initiation, execution, monitoring, analysis, regulatory filing, and publication. **Specifically, The Clinical Director May… more
    Merck (01/15/25)
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  • Licensing Support Specialist - Cosmetology…

    State of Massachusetts (Boston, MA)
    …Produce certified statements of licensure. * At the direction of the Executive Director ("ED") or Associate Deputy Commissioner, assist with the scheduling of ... Licensure (DOL), an agency within the Office of Consumer Affairs and Business Regulation (OCABR), protects consumers by making...under the guidance and supervision of the ED or Associate Deputy Commissioner. * Maintain files and records of… more
    State of Massachusetts (11/05/24)
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