• Sr. Specialist, Project Management…

    Merck (West Point, PA)
    …in support of clinical supply planning group (eg, process improvement initiatives, subject matter expert roles, cross functional projects, etc.) - ... (GCS) organization is accountable for managing the 'end-to-end' integrated clinical supply chain across the full Research ...proven ability to execute on collaborative projects and develop subject matter expertise - Knowledge of order… more
    Merck (10/23/25)
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  • Oncology Late Stage Clinical Scientist (Non

    Pfizer (Collegeville, PA)
    …level workgroups aimed at optimizing PFE clinical development procedures; may be a subject matter expert or business process owner for a relevant SOP ... programs within the Late-Stage Oncology portfolio. **KEY RESPONSIBILITIES** + Clinical development expert for assigned studies...a relevant Science discipline and minimum of 2 years Clinical Research experience in industry/CRO, **OR** +… more
    Pfizer (11/05/25)
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  • Senior Paralegal - St. Francis

    Bon Secours Mercy Health (Greenville, SC)
    …in one or more markets and/or functions (eg Supply Chain); and (2) Serves as a Paralegal subject matter expert ( SME ) role for the legal network. The ... to specific business needs. + Serves as a Paralegal SME Expert or Consultant. Paralegal SME...annual basis. Education may pertain to a particular practice area/ subject matter or may be geared to… more
    Bon Secours Mercy Health (10/31/25)
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  • Principal Scientist, Clinical Assay…

    CSL Behring (Waltham, MA)
    …and define next steps across areas of expertise for often complex issues. Recognized subject matter expert in job area typically obtained through advanced ... in the area of bioanalytical and biomarker assays to support nonclinical and clinical studies . This role will support the external tactical execution of… more
    CSL Behring (11/01/25)
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  • Director, Clinical Pharmacology Lead

    Organon & Co. (Jersey City, NJ)
    …to market opportunities. + Represent the Clinical Pharmacology function or serve as subject matter expert for translational medicine and clinical ... briefing books, IND subsections, submission modules and other regulatory documents. + Provide clinical pharmacology subject matter expertise and lead the… more
    Organon & Co. (10/02/25)
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  • Director Clinical Assay Strategy,…

    CSL Behring (Waltham, MA)
    …turn around times, assay transfers, budgets, and resource allocation.​ Scientific Oversight​ Recognized subject matter expert in job area typically obtained ... report to the Senior Director, Global Lead and Head Research and Clinical Bioanalytics. You will lead...of bioanalytical and biomarker assays to support nonclinical and clinical studies . This role requires a strategic… more
    CSL Behring (11/01/25)
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  • Senior Program Officer, Clinical Immunology

    Bill and Melinda Gates Foundation (Seattle, WA)
    …Provide Subject Matter Expertise: + Serve as a thought partner and subject matter expert to foundation colleagues and as resource to grantees and ... You interact actively with the international biomedical scientific and clinical research community and are expected to...maintain a cutting-edge understanding of the field, provide deep subject matter expertise, act as thought-partner both… more
    Bill and Melinda Gates Foundation (09/03/25)
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  • Staff Engineer Research and Development…

    Cordis (Santa Clara, CA)
    studies concisely. Participates in the regulatory submission process as a subject matter expert . Supports regulatory by providing technical ... individual technical expert , conceives or is assigned, plans, and conducts research in problem areas of considerable scope and complexity + Anticipates, plans,… more
    Cordis (10/23/25)
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  • AAT Research and Telemetry Technician

    Alaka'ina Foundation Family of Companies (Frederick, MD)
    …BSL-3, and BSL-4 biocontainment laboratory environments. Workload is approximately twenty (20) research studies per year. + Operate and maintain the telemetry ... BSL-3, and BSL-4 biocontainment laboratory environments. Workload is approximately twenty (20) research studies per year. + Assist to generate, characterize, and… more
    Alaka'ina Foundation Family of Companies (10/07/25)
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  • Senior Director and Head of Clinical

    Takeda Pharmaceuticals (Cambridge, MA)
    …a culture of sustainable compliance. Represents Takeda as a clinical quality subject matter expert during health authority inspections of the sponsor. ... with at least 5 years of Quality/Compliance experience. + Advanced knowledge of clinical research (GCP), pharmacovigilance (GVP) and medical throughout R&D and… more
    Takeda Pharmaceuticals (10/25/25)
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