• Director , SM Medical Affairs, LSM Platform

    BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
    …have strong strategic and operational experience with product development including clinical trial strategy, design and execution, demonstrated productivity in ... the business unit Vice President of Medical Affairs, the Director of Medical Affairs has the responsibility to support...staff will be an advantage + Needs knowledge of clinical trial design, statistics, and data analysis.… more
    BD (Becton, Dickinson and Company) (06/18/25)
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  • Associate Director , Global Regulator…

    Bristol Myers Squibb (Princeton, NJ)
    …DSURs, etc. + Co-lead the cross-functional rapid response teams to respond to Clinical Trial Application (CTA) queries on new protocols and protocol amendments ... and unique perspectives in a supportive culture, promoting global participation in clinical trials , while our shared values of passion, innovation, urgency,… more
    Bristol Myers Squibb (08/28/25)
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  • US Executive Director , Medical Affairs,…

    Merck (Trenton, NJ)
    …and leads research and scientific field medical capabilities in alignment with Global Clinical Trial Operations (GCTO) and the broader Global Clinical ... **Job Description** The Executive Director (ED) for US Medical Affairs (USMA) understands...key pillars of objectives: 1.) Scientific Exchange 2.) Company Trials 3.) Investigator-Sponsored Programs 4.) Congresses 5.) Insights +… more
    Merck (08/20/25)
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  • Senior Principal Scientist/Associate…

    Bristol Myers Squibb (Princeton, NJ)
    …and large collaborations with academia and industry partners to identify biobanks, clinical trials and existing databases to collate multi-parameter genomic, ... cross-functional teams. Excellent communication and collaboration skills. + Prior experience with clinical trials preferred + Strong track record of high-quality… more
    Bristol Myers Squibb (08/14/25)
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  • Senior Director Biostatistics

    Bristol Myers Squibb (Princeton, NJ)
    …experience) in statistics or biostatistics or related scientific field with clinical trials , drug development, pharmaceutical industry or healthcare experience ... + Demonstrate expertise in applying knowledge of general and cutting edge statistical / clinical trials methodology to solve complex statistical problems in the … more
    Bristol Myers Squibb (07/15/25)
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  • Scientific Director /Senior Scientific…

    Bristol Myers Squibb (Princeton, NJ)
    …and unique perspectives in a supportive culture, promoting global participation in clinical trials , while our shared values of passion, innovation, urgency, ... some of the brightest minds in biopharma. **Position Summary** The Scientific Director /Senior Director , CMC Team Leader is responsible for developing and… more
    Bristol Myers Squibb (08/29/25)
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  • Director , Cell Therapy WW Medical,…

    Bristol Myers Squibb (Princeton, NJ)
    …and unique perspectives in a supportive culture, promoting global participation in clinical trials , while our shared values of passion, innovation, urgency, ... more: careers.bms.com/working-with-us . **Position Overview** Reporting to the Executive Director , Cell Therapy Multiple Myeloma (MM)/Solid Tumor Pipeline Lead, the… more
    Bristol Myers Squibb (08/20/25)
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  • Director , Real World Research

    J&J Family of Companies (Titusville, NJ)
    …is required. + Expertise with a broad range of biostatistical, econometric, clinical trial , and/or epidemiological research methods required + Expertise and ... Locations:** Titusville, New Jersey, United States of America **Job Description:** ** Director , Real World Research - Scientific Evidence & Policy Research (SEPR)**… more
    J&J Family of Companies (08/23/25)
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  • Director , PV Medical Surveillance

    Taiho Oncology (Princeton, NJ)
    …opportunity to work with cross functional team for early to late-stage global clinical trials and post-marketing products. You will contribute to the growth ... products assigned, including review and analysis of safety data from clinical trials and from post-marketing sources, providing medical expertise to assigned… more
    Taiho Oncology (07/12/25)
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  • Director , Global Regulatory Affairs…

    Sanofi Group (Morristown, NJ)
    …endpoints, offering strategic input into the design of Phase 2 and Phase 3 clinical trials . + Assess opportunities for the integration of patient experience data ... **Job Title:** Director , Global Regulatory Affairs - Global Labeling Strategy...early in product development by providing regulatory input into clinical development plans, including guidance on Phase 2 and… more
    Sanofi Group (06/27/25)
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