• Associate Director , Regulatory…

    Sumitomo Pharma (Providence, RI)
    …a dynamic, highly motivated, and experienced individual for the position of **Associate Director , Regulatory Affairs (Oncology).** The Associate Director ... is part of the Global Regulatory Affairs (GRA) team based in the US. He/She will...Ideally with a minimum of 4 years focused in regulatory affairs + Oncology product development experience… more
    Sumitomo Pharma (10/11/25)
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  • Director , Regulatory Affairs

    Sumitomo Pharma (Providence, RI)
    …are currently seeking a dynamic, highly motivated, and experienced individual for the position of ** Director Regulatory Affairs ** . The Director is part ... of the Global Regulatory Affairs (GRA) team based in the US. He/she will...pharmaceutical industry with minimum of 8 years focused in regulatory affairs . + Master's degree required (preferably… more
    Sumitomo Pharma (09/09/25)
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  • Senior Medical Science Liaison

    Cardinal Health (Providence, RI)
    …joins a team of medical affairs professionals who report to the Sr Director of Regulatory & Medical Affairs . **Responsibilities:** + Collaborate across ... hours. We also provide customers the support they need in regulatory compliance, reimbursement, continuing education, information management and other crucial areas,… more
    Cardinal Health (10/31/25)
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  • Associate Director , Small Molecule…

    Otsuka America Pharmaceutical Inc. (Providence, RI)
    …cross-functionally with analytical team members, process chemistry, formulation development, regulatory affairs , quality assurance, and other departments to ... **Associate Director , Small Molecule Analytical Development** + Lead and...and drug product ensuring compliance with relevant ICH and regulatory guidelines + Develop and implement stability study protocols… more
    Otsuka America Pharmaceutical Inc. (08/27/25)
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  • Director , Global Value Evidence Operations

    Otsuka America Pharmaceutical Inc. (Providence, RI)
    **Position Summary:** The Director GVE Operations oversee and coordinates projects within the department to ensure alignment with organizational goals. This role is ... other integrated data generation initiatives. This position reports to the Senior Director , Global Integrated Evidence & Innovation Operations and can be based in… more
    Otsuka America Pharmaceutical Inc. (09/13/25)
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  • Senior Director , MSAT Biologics

    Otsuka America Pharmaceutical Inc. (Providence, RI)
    …appropriate. + Collaborate with cross-functional teams including R&D, Quality Assurance, Regulatory Affairs , and Operations to align strategies and optimize ... **Position Overview:** The Senior Director , MSAT Biologics provides strategic and technical leadership...validation lifecycle (PPQ, CPV, etc.) ensuring compliance with global regulatory standards. + Establish and oversee robust Continued Process… more
    Otsuka America Pharmaceutical Inc. (10/13/25)
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  • Director , HCP Marketing Lead

    Otsuka America Pharmaceutical Inc. (Providence, RI)
    **Position Summary** The Director , HCP Marketing Lead guides the healthcare provider (HCP) engagement strategy for Centanafadine, a novel launch product for ADHD. ... engagement to drive awareness, adoption, and utilization among HCPs. The Director will work cross-functionally with sales, market access, medical affairs… more
    Otsuka America Pharmaceutical Inc. (11/01/25)
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  • Manager, Government Relations, NA State and Local

    Lenovo (RI)
    …seeking an experienced professional to manage the company's state and local governmental affairs strategy in the US The successful candidate will work closely with ... and local levels. The position will report to the Director , Government Relations, the incumbent will closely interact with...the legal department, advise business units on policy and regulatory matters that may impact the development or deployment… more
    Lenovo (10/30/25)
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  • Trial Master File (TMF) Specialist Oncology

    Sumitomo Pharma (Providence, RI)
    …ensure system validation is maintained. + Work closely with Clinical Operations and Regulatory Affairs to ensure compliance with regulatory requirements. + ... (TMFs) ready for audits and inspections. Partnering with the Associate Director , Clinical Business Operations, the specialist ensures accountable functions follow… more
    Sumitomo Pharma (11/05/25)
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