• Pediatric Pharmacy Resident, PGY2

    Vanderbilt University Medical Center (Nashville, TN)
    …Vanderbilt University Medical Center Post‐Graduate Year One (PGY1) Pharmacy Residency program is a 12-month, full‐time residency, accredited by the American Society ... prepared to pursue and complete PGY2 residency training. The mission of our program includes developing a core skill set in drug information and literature… more
    Vanderbilt University Medical Center (01/15/26)
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  • Senior Director, Global Regulatory Lead…

    Bristol Myers Squibb (Princeton, NJ)
    …key member of the GRSP Extended Leadership Team to ensure the development , implementation, and alignment of regulatory strategies across projects and the ... company-wide projects and initiatives. + Support due diligence and business development assessments. + Working with regional regulatory staff as Global Regulatory… more
    Bristol Myers Squibb (01/17/26)
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  • Director - Clinical Research Scientist - Global…

    Lilly (Indianapolis, IN)
    …considerations are effectively integrated into local business activities and global development plans. **Key Responsibilities** **1. Business & Customer Support** + ... support scientific booth activities. + Contribute to data analyses, publication development , and Clinical Trial Registry reporting. **3. Clinical Planning** + Align… more
    Lilly (01/16/26)
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  • Clinical Scientist

    Sanofi Group (Morristown, NJ)
    …of the clinical strategic plan with the appropriate governance committees. + Support program strategy including clinical development plan and regulatory needs. + ... Team:** _The Lunsekimig project team is part of Early Development in the Inflammation & Immunology Therapeutic Area at...**About You** Education and experience: + Advanced degree preferred ( PharmD or PhD scientist or Biomedical Science master with… more
    Sanofi Group (01/17/26)
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  • Vice President, Regulatory Affairs

    Xeris Pharmaceuticals, Inc. (Chicago, IL)
    …executing the company's global regulatory strategy to support clinical development , product approvals, lifecycle management, and ongoing compliance. The incumbent ... strategic yet hands-on leader with deep experience in drug development , submissions, labeling, advertising and promotion, and post-approval compliance.… more
    Xeris Pharmaceuticals, Inc. (12/30/25)
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  • Director, Heva (HEOR) Business Partner

    Sanofi Group (Cambridge, MA)
    …of the highest unmet needs. Sanofi Specialty Care has pioneered the development and delivery of transformative therapies for patients affected by debilitating ... people's lives. **Main Responsibilities:** This role will be responsible for development of Health Economic and Outcomes Research (HEOR) strategy and execution… more
    Sanofi Group (12/25/25)
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  • Medical Director, Global Strategy Lead Rare…

    Otsuka America Pharmaceutical Inc. (Providence, RI)
    …shaping the strategic processes and planning for assets in across phases of development within the Rare Disease portfolio. This position manages the unique challenge ... Narrative** + Provide key medical input into the initial development of the Target Reimbursable Product Profile as well...for early assets + Manage assigned Rare Disease medical program budgets in partnership with the Rare Disease Medical… more
    Otsuka America Pharmaceutical Inc. (12/16/25)
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  • Director, Oncology Early

    Pfizer (Cambridge, MA)
    **POSITION SUMMARY** You will lead and coordinate the development of multiple studies of novel biological and small molecules for first in human (FIH), proof of ... You will work in close collaboration with the Global Development Lead (GDL)and members of the development ...**MINIMUM QUALIFICATIONS / KEY SKILLS** + Relevant PhD or PharmD and a minimum of 5 years of experience… more
    Pfizer (12/13/25)
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  • Director, Regulatory Affairs CMC

    Taiho Oncology (Princeton, NJ)
    …evolving needs of patients. Advanced technology, a world-class clinical development organization, and state-of-the-art facilities: these and other resources empower ... provides strategic regulatory guidance especially for CMC during drug development , approval and post approval processes and commercialization, in coordination… more
    Taiho Oncology (12/09/25)
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  • Exec Director, Regulatory Affairs-Combination…

    Gilead Sciences, Inc. (Washington, DC)
    …member of Gilead's team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we ... regulatory expectations. Champion regulatory innovation and novel approaches to accelerate development and approval timelines. Provide guidance to PDM Teams and… more
    Gilead Sciences, Inc. (12/03/25)
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