• Director Clinical

    Tufts Medicine (Burlington, MA)
    …as a Registered Nurse 3. Five (5) years relevant experience in the management of Clinical Documentation Integrity team 4. CCDS certification through ACDIS or ... advisors and leaders. The Director oversees the manager and clinical documentation specialists (CDSs) in planning, implementing improvements, and… more
    Tufts Medicine (07/04/25)
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  • Senior Director Clinical Revenue

    Tufts Medicine (Burlington, MA)
    …MA **Job Overview** This role oversees the functions and personnel in the Clinical Documentation Integrity (CDI), Coding, HIM Operations, and Utilization ... Integrity , Patient Access; Patient Financial Services (PFS), and Revenue Integrity providing direction on clinical documentation and coding-related… more
    Tufts Medicine (07/04/25)
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  • Director , Prospective + Concurrent Risk…

    Datavant (Boston, MA)
    …party integrations. + Balance innovation with compliance, audit defensibility, and clinical integrity across all product decisions. **Execution & Delivery:** ... provider documentation teams, coders, or concurrent review vendors. + Clinical experience or deep engagement with clinician stakeholders. + Familiarity with… more
    Datavant (08/08/25)
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  • Director , Third Party Data Acquisition

    Takeda Pharmaceuticals (Boston, MA)
    Director , Third Party Data Acquisition based remotely reporting to the Senior Director , Clinical Trial Configuration. At Takeda, we are transforming the ... Data Acquisition is responsible for timely and high-quality delivery of systems and documentation for non-EDC data in support of Clinical studies. + Conduct… more
    Takeda Pharmaceuticals (09/10/25)
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  • Director , Billing Compliance

    Dana-Farber Cancer Institute (Brookline, MA)
    …corrective actions. + **Training and Education:** Develops curriculum and delivers clinical documentation , coding and billing education programs for physicians, ... a dotted line reporting relationship to the VP, Revenue Performance Management, the Director of Billing Compliance ensures the integrity and accuracy of billing… more
    Dana-Farber Cancer Institute (07/01/25)
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  • Director , Regulatory Affairs

    Sumitomo Pharma (Boston, MA)
    …relationship with colleagues, fostering collaboration, and idea sharing + Reviews nonclinical, clinical and CMC documentation (eg nonclinical study reports, ... general product development in the pharmaceutical industry + Experience reviewing nonclinical, clinical and CMC documentation (eg nonclinical study reports, … more
    Sumitomo Pharma (09/09/25)
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  • Assistant Director for Federal Grants

    State of Massachusetts (Boston, MA)
    …seeking a highly skilled fiscal and compliance leader to serve as the Assistant Director of Federal Grants within the Accounting Office. This is a key leadership ... from more than a dozen federal agencies. The Assistant Director will play a critical role in ensuring the... will play a critical role in ensuring the integrity of DPH's financial operations by overseeing compliance with… more
    State of Massachusetts (09/02/25)
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  • Executive Director , Regulatory Science

    Orchard Therapeutics (Boston, MA)
    Location: Boston, MA Main responsibilities The Executive Director (ED) Regulatory Science will actively support, and serve as senior advisor to, the program ... contingency plans as needed. . Ensure effective cross-functional collaboration with the Clinical department (including Clinical Science, Clinical Operations,… more
    Orchard Therapeutics (09/09/25)
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  • Associate Director , Global Regulator…

    Bristol Myers Squibb (Cambridge, MA)
    …their personal lives. Read more: careers.bms.com/working-with-us . **Associate Director , Global Regulatory Strategy, Neuroscience** **Position Summary:** The ... HAs for respective regions/countries + Prepare content for regulatory strategic documentation and Regulatory Project Reviews. Align regulatory plans with commercial… more
    Bristol Myers Squibb (09/12/25)
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  • Director , Global Regulatory Labeling…

    Takeda Pharmaceuticals (Boston, MA)
    …in order to bring life-changing therapies to patients worldwide. Join Takeda as Director , Global Regulatory Labeling Strategy where you will be responsible for the ... approval from all relevant functional areas with appropriate annotations and supporting documentation . + In a highly efficient manner, develops and executes a… more
    Takeda Pharmaceuticals (09/10/25)
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