• Associate Director , Clinical Data…

    Bristol Myers Squibb (Princeton, NJ)
    …This position will be based in San Diego, CA or Lawrenceville, NJ. **Summary:** The Associate Director , Clinical Data Management, will play a crucial role in our ... management tools; ability to learn new systems as needed. + Contribute to SOP development and updates to meet regulatory compliance and operational needs. + 10% of… more
    Bristol Myers Squibb (05/29/25)
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  • Associate Director Quality Assurance…

    BeOne Medicines (Pennington, NJ)
    …management of Compliance programs for the Hopewell, NJ site. Programs which require development under the QMS include, but are not limited to market action, ... as needed for Quality Assurance Agreement authoring and vendor qualification. + Development of all necessary SOPs, ensuring regulatory compliance in conjunction with… more
    BeOne Medicines (05/08/25)
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  • Associate Director , Program Lead…

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …Years of related experience, including Project Management, Clinical Supply Management, and/or Pharmaceutical Development or technical writing required + 1 or ... Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address diversified, unmet medical… more
    Daiichi Sankyo Inc. (05/08/25)
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  • Senior Scientist/ Associate Director

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address diversified, unmet medical ... This position makes decisions with consultation. **Responsibilities:** + **Planning for Development :** Manages multiple CMC development projects. Leads… more
    Daiichi Sankyo Inc. (05/15/25)
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  • CDx Associate Director , Global…

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address diversified, unmet medical ... immune disorders. **Summary:** Responsibility for regulatory strategy to support the development of biomarkers, companion diagnostic tests and other devices to… more
    Daiichi Sankyo Inc. (05/29/25)
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  • Associate Director , Companion…

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …with BS/BA + Demonstrated track record of success working on multidisciplinary pharmaceutical /diagnostic development teams required + Understanding of the IVD ... Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address diversified, unmet medical… more
    Daiichi Sankyo Inc. (04/29/25)
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  • Associate Director , Omnichannel…

    Otsuka America Pharmaceutical Inc. (Trenton, NJ)
    …Center at: https://www.ic3.gov , or your local authorities. Otsuka America Pharmaceutical Inc., Otsuka Pharmaceutical Development & Commercialization, ... retrieval. This position specifically entails the conceptualization, prototyping and development of next generation advanced analytics model-based decision engines… more
    Otsuka America Pharmaceutical Inc. (05/16/25)
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  • Associate Director , Labeling

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address diversified, unmet medical ... complexity including post marketing projects and those involving 3rd party development . This position partners with GRLs and Clinical Safety Pharmacovigilance (CSPV)… more
    Daiichi Sankyo Inc. (05/09/25)
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  • Associate Director , Quality Control…

    BeOne Medicines (Pennington, NJ)
    …Competencies, Knowledge and Skill Requirements_** + Scientific degree (ideally pharmacy, pharmaceutical sciences, chemistry or related). + Minimum of 8 years' ... in biological drug product quality control in an FDA-regulated biotechnology, pharmaceutical company with progressive levels of responsibility are required. +… more
    BeOne Medicines (05/23/25)
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  • Associate Director , Regulatory…

    Bristol Myers Squibb (Princeton, NJ)
    …+ Leadership responsibility for global regulatory strategy to support the development of biomarkers, companion diagnostic tests, digital health and other devices ... to enhance the value of our pharmaceutical products across therapeutic areas + Responsible for understanding...to global Health Authority (HA) queries. + Ensure global development plans will meet global regulatory requirements by soliciting… more
    Bristol Myers Squibb (04/27/25)
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