• Associate Director

    Sumitomo Pharma (Annapolis, MD)
    …currently seeking 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 primarily function as a regional regulatory leader… more
    Sumitomo Pharma (10/11/25)
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  • Director , Strategic Planning & Operations…

    Otsuka America Pharmaceutical Inc. (Annapolis, MD)
    The Director , Strategic Planning & Operations is a pivotal role within the Medical Excellence & Operations team within Global Medical Affairs . This role is ... the asset lifecycle. This role reports directly into the Executive Director , Medical Excellence and Operations. **Job Description** **Key Responsibilities Include:**… more
    Otsuka America Pharmaceutical Inc. (11/14/25)
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  • Associate Director

    Otsuka America Pharmaceutical Inc. (Annapolis, MD)
    The Associate Director of Regulatory Intelligence leads the collection and dissemination of regulatory intelligence and collaborates with SMEs to ... + Build professional network with key stakeholders outside of Global Regulatory Affairs to identify regulatory intelligence needs and strengthen and… more
    Otsuka America Pharmaceutical Inc. (11/13/25)
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  • Associate Director , Congress…

    Otsuka America Pharmaceutical Inc. (Annapolis, MD)
    The Associate Director , Congress and Medical Education Strategy & Execution is responsible for executing and contributing to the global medical strategy and ... patient outcomes through deep scientific understanding and collaborative partnerships. The Associate Director partners closely with global and regional… more
    Otsuka America Pharmaceutical Inc. (11/14/25)
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  • Associate Director , Scientific…

    Otsuka America Pharmaceutical Inc. (Annapolis, MD)
    The Associate Director , Scientific Communications manages the execution of the core scientific and medical communications strategy for the relevant therapeutic ... accurate, evidence-based, and compliant with internal policies and external regulatory requirements. + Collaborate cross-functionally with Medical Affairs ,… more
    Otsuka America Pharmaceutical Inc. (11/14/25)
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  • Program & Technical Advisor (Sr.…

    Guidehouse (Hanover, MD)
    …Software, Assay chemistry, microbiology, virology, immunology **_Programmatic/Technical Advisor_** - Associate Director + **Doctoral degree** in biological ... FDA/ICH guidelines and CDISC data standards + Experience in pharmaceutical industry regulatory affairs and/or quality assurance and/or quality control + Direct… more
    Guidehouse (11/09/25)
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  • Associate Director , Small Molecule…

    Otsuka America Pharmaceutical Inc. (Annapolis, MD)
    ** Associate Director , Small Molecule Analytical Development** + Lead and oversee phase appropriate method development and optimization for drug substance and ... cross-functionally with analytical team members, process chemistry, formulation development, regulatory affairs , quality assurance, and other departments to… more
    Otsuka America Pharmaceutical Inc. (08/27/25)
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  • Instructor for Master of Science (MS)…

    University of Maryland, Baltimore (Baltimore, MD)
    …in the MS in Regulatory Science program, with a focus on introductory and regulatory affairs aspects of the program, as well as another aspect of the program ... AREAS OF EXPERTISE AND EXPERIENCE_* Regulatory science, including introductory and regulatory affairs aspects, as well deep knowledge in another aspect (eg… more
    University of Maryland, Baltimore (10/14/25)
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  • Manager, Medical Core Content - CNS

    Otsuka America Pharmaceutical Inc. (Annapolis, MD)
    …internal and external regulations. This position reports directly to the Associate Director , CNS Scientific Communications. **Job Description** **Key ... Include:** **Core Content Development** + Under the guidance of the Associate Director , Medical Communications, draft and maintain high-priority, foundational… more
    Otsuka America Pharmaceutical Inc. (11/14/25)
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  • Trial Master File (TMF) Specialist Oncology

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