• Merck & Co. (Rahway, NJ)
    …to pursue and subsequent study design, initiation, execution, monitoring, analysis, regulatory filing, and publication.Specifically, The Senior Director May Be ... Job DescriptionThe Senior Director (Sr. Principal Scientist) has primary responsibility for...execution of clinical studies. Work closely with a cross-functional group of experts in commercialization, regulatory affairs,… more
    HireLifeScience (10/25/25)
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  • Merck & Co. (Rahway, NJ)
    …through research and innovation. Through clinical trials and surveillance, we ensure the safety and efficacy of our existing and pipeline products to produce safe, ... effective, innovative medicine.The Clinical Director is responsible for protocol development and medical/ scientific...new or marketed drugs in the Vaccines Clinical Research group . They will be responsible for all phases of… more
    HireLifeScience (10/25/25)
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  • Merck & Co. (Rahway, NJ)
    …career. Responsibilities include, but are not limited to: Work closely with the group Director to shape and execute strategy for biological characterization in ... and supervise junior colleagues; coach, and develop talent within the group , contribute to employee career development; build independent ownership and evolution… more
    HireLifeScience (10/18/25)
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  • Sr Director , Global Leader,…

    J&J Family of Companies (Raritan, NJ)
    …profoundly impact health for humanity. Learn more at https://www.jnj.com **Job Function:** Regulatory Affairs Group **Job Sub** **Function:** Regulatory ... Description:** Johnson & Johnson is recruiting for the **Sr Director , Global Leader, Regulatory Data & Process...IDMP, SPOR, structured content), required. + Understanding of how regulatory processes interconnect with R&D, clinical, safety more
    J&J Family of Companies (10/25/25)
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  • Director , Field Reimbursement - Vaccines

    Sanofi Group (Morristown, NJ)
    **Job Title:** Director , Field Reimbursement - Vaccines **Location:** Remote/Field **About the Job** The Director , Reimbursement Education Liaison role will ... of healthcare around our portfolio of vaccines. In this role, the Director , Reimbursement Education Liaison (DREL) will establish and sustain reliable company… more
    Sanofi Group (09/23/25)
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  • Executive Director , Therapeutic Area…

    J&J Family of Companies (Raritan, NJ)
    …of America **Job Description:** Johnson & Johnson, is recruiting for a Executive Director , Therapeutic Area Safety Head, Cardiopulmonary to be located in ... transparency, and communication. + Act ethically and responsibly to ensure patient safety is paramount + Provide leadership in regulatory authority interactions… more
    J&J Family of Companies (10/04/25)
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  • Associate- Director , Human Factors…

    Sanofi Group (Morristown, NJ)
    **Job Title:** Associate- Director , Human Factors and Usability Engineering **Location:** Morristown, NJ Cambridge, MA **About the Job** We deliver 4.3 billion ... diseases and bring hope to patients and their families. The Associate Director will be responsible for leading and executing HFUE activities, continuous HFUE… more
    Sanofi Group (10/25/25)
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  • Director , SM Medical Affairs, Specimen…

    BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
    …meet regulatory requirements, and support appropriate product use. The Director of Medical Affairs needs to have experience in understanding the preanalytical ... the business unit Vice President of Medical Affairs, the Director of Medical Affairs has the responsibility to support...teams, and assessment of clinical evidence requirements to meet regulatory , safety and efficacy criteria and support… more
    BD (Becton, Dickinson and Company) (09/20/25)
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  • Senior Clinical Director , Oncology Early…

    Merck (Rahway, NJ)
    regulatory reporting, and publication. **Responsibilities:** Specifically, the Senior Director may be responsible for: Analyzing and summarizing the clinical ... changes the way we approach serious diseases. The Senior Director will report to an Associate Vice President in...execution of clinical studies. Work closely with a cross-functional group of experts in commercialization, regulatory affairs,… more
    Merck (10/25/25)
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  • Associate Director , ICSR Management Team…

    Ascendis Pharma (Princeton, NJ)
    Safety Databases (Argus preferred) + Experience with MedDRA coding and global safety reporting regulatory requirements. + Expert knowledge of FDA safety ... employees to grow and develop their skills. The Associate Director , ICSR Management Team reports to the Director... regulatory guidance documents; working knowledge of global safety regulations. + Ability to travel up to 20%… more
    Ascendis Pharma (10/09/25)
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