• Daiichi Sankyo, Inc. (Bernards, NJ)
    …research areas centered around rare diseases and immune disorders. Summary: The Senior Director, Clinical Safety , will lead the development and implementation ... of integrated project /product risk management strategies aimed at achieving the optimum...the CSPV on the Global Product Team or other cross- functional teams providing the safety leadership and… more
    HireLifeScience (12/05/25)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    …media capabilities. This position will also manage and oversee Product Safety practices, monitoring and audits across all Patient Support Programs, including ... in order to accomplish objectives. Relationship Reports to the Director, Patient Safety Data Acquisition & Support. Interacts with colleagues within Patient Support… more
    HireLifeScience (11/25/25)
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  • Bayer (Whippany, NJ)
    …brilliant and diverse minds to make a real difference, there’s only one choice. Senior Director, Digital Governance & LMR Lead The Senior Director, Digital ... Governance & Legal Medical Review (LMR) supports Medical Governance processes enabling cross- functional teams to be accountable for the delivery of high quality,… more
    HireLifeScience (12/19/25)
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  • Merck & Co. (Rahway, NJ)
    …BPR&D as a upstream bioprocess expert/co-leader in internal and cross- functional project teams.Supervise, coach, and develop talent within ... early adoption of novel process technologies.Contribute to strategic initiatives; work with senior leaders to establish overall project strategy and guide teams… more
    HireLifeScience (12/18/25)
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  • Merck & Co. (MA)
    Job DescriptionThe Senior Director (Sr. Principal Scientist) has primary responsibility for the strategic planning and directing clinical research activities ... in Immunology. With a focus on late-stage development, the Senior Clinical Director will manage the entire cycle of...the clinical findings from studies to support decisions regarding safety and efficacy as well as new drug applications,… more
    HireLifeScience (12/20/25)
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  • Merck & Co. (Durham, NC)
    … and Health, Process Improvement Projects, Productivity Improvements, Project Management, Regulatory Audits, Regulatory Compliance, Sterile Manufacturing, System ... involving any of the following: Regulatory compliance with internal interpretations Manage project strategy for the Durham Site to achieve Net Zero goals based… more
    HireLifeScience (12/19/25)
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  • Merck & Co. (Rahway, NJ)
    Job DescriptionThe Senior Director (Sr. Principal Scientist) has primary responsibility for the planning and directing clinical research activities involving new or ... span all phases of clinical development (pre-clinical to post-licensure). The Senior Director will manage the entire cycle of late-stage clinical development… more
    HireLifeScience (12/20/25)
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  • Merck & Co. (Durham, NC)
    Safety and Health, Process Improvement Projects, Productivity Improvements, Project Management, Regulatory Audits, Sterile Manufacturing, System Maintenance, Team ... for plant engineeringEnsures utility operations daily priorities and schedules project /work meeting the criteria established by site objectives.Support / lead… more
    HireLifeScience (12/19/25)
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  • Merck & Co. (Rahway, NJ)
    …where all employees can thrive.Responsibilities include but are not limited to:Partner with functional area project teams and subject matter experts to establish ... risks and associated solutions to ensure on time delivery of project deliverables.Collaborate with cross- functional teams to support technology transfer,… more
    HireLifeScience (12/06/25)
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  • Merck & Co. (Boston, MA)
    Job DescriptionOur Clinical and Pharmacovigilance teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new ... to produce safe, effective, and innovative medicines, and we work with cross- functional colleagues in Global Medical and Scientific Affairs and Global Policy to… more
    HireLifeScience (12/02/25)
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