• Senior Project Manager, Cell Therapy…

    Bristol Myers Squibb (Princeton, NJ)
    …leads matrixed cross-functional project management teams and projects within the Medical Affairs Cell Therapy Organization. This role reports directly ... serving as a strategic and operational partner within the Cell Therapy Medical organization to deliver key portfolio priorities. Responsibilities include global and… more
    Bristol Myers Squibb (08/28/25)
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  • Director, Global Regulatory Affairs

    Sanofi Group (Morristown, NJ)
    …labeling leadership to cross-functional teams (Regulatory Strategy, Clinical Development, Medical Affairs , Pharmacovigilance, Market Access ). + Contribute ... **Job Title:** Director, Global Regulatory Affairs - Global Labeling Strategy **Location** : Morristown,...was possible. Ready to get started? **Main Responsibilities** + Lead the development, maintenance, and alignment of global labeling… more
    Sanofi Group (06/27/25)
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  • Associate Director, Commercial Regulatory…

    Bristol Myers Squibb (Princeton, NJ)
    …+ Provides regulatory advice, risk assessment and mitigation strategies to Commercial Teams, Medical Affairs , Public Affairs , Value Access and Payment, and ... compliance with sub part e and 2253 regulations + Lead training for Commercial teams on sub part e,...maintain strong working relationships with internal customers, including Commercial, Medical , Public Affairs , Legal and Compliance +… more
    Bristol Myers Squibb (08/25/25)
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  • Associate Director, Global Regulatory…

    Sanofi Group (Morristown, NJ)
    …teams, including Global Regulatory Affairs , Clinical Development, Safety, and Medical Affairs , to ensure labeling content reflects scientific integrity, ... **Job Title:** Associate Director, Global Regulatory Affairs - Global Labeling Strategy **Location** : Morristown,...was possible. Ready to get started?​ **Main Responsibilities** + Lead the preparation, review, and maintenance of global labeling… more
    Sanofi Group (06/27/25)
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  • Executive Director, WW Medical Oncology,…

    Bristol Myers Squibb (Princeton, NJ)
    …project managers who are charged with partnering with colleagues in WW Medical Affairs or in other functions to lead or support the business operations and ... planning and execution of activities for the Oncology WW Medical Affairs Department, including brand and ...Affairs , assess capabilities, and drive continuous improvement. + Lead special projects requiring medical leadership and… more
    Bristol Myers Squibb (08/29/25)
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  • Associate Director, Regulatory Affairs

    United Therapeutics (Trenton, NJ)
    …or pharma regulatory experience with a Bachelor's Degree in life sciences, quality, regulatory affairs or a related area of study or 10+ years of biologic or pharma ... with a Master's Degree in life sciences, quality, regulatory affairs or a related area of study or 7+...in successfully navigating regulatory submissions + Proven ability to lead and influence data-driven strategy planning and implementation +… more
    United Therapeutics (08/10/25)
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  • Associate Director, Global Regulatory…

    Organon & Co. (Jersey City, NJ)
    **Job Description** **The Position** The Associate Director, Global Regulatory Lead (GRL), reporting to the Executive Director, Senior Director or Director, Global ... of contact or the EU-procedure regulatory expert on those projects. + Lead the Global Regulatory Teams, which coordinates cross-functional regulatory support for… more
    Organon & Co. (07/26/25)
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  • Associate Director, Regulatory Affairs

    BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
    …preferred; medical training preferred. + Minimum 8 years of regulatory affairs experience within the pharmaceutical or medical device industries, ideally ... **Job Description Summary** As Associate Director, Regulatory Affairs , you will be responsible for leading RA...of possible** BD is one of the largest global medical technology companies in the world. Advancing the world… more
    BD (Becton, Dickinson and Company) (08/27/25)
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  • Associate Principal Scientist, Regulatory…

    Organon & Co. (Jersey City, NJ)
    …regulations and guidances, and Organon procedures. The Associate Principal Scientist will lead the preparation and submission of CMC dossiers for programs in ... limited to: **Responsibilities** + Serve as the CMC Product Lead or support the CMC Product Lead ...processes and systems. + Demonstrate an understanding of regulatory affairs and apply this understanding to the benefit of… more
    Organon & Co. (07/22/25)
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  • Director, Regulatory Affairs -- Therapeutic…

    Gilead Sciences, Inc. (Parsippany, NJ)
    …and help create possible, together. **Job Description** **POSITION OVERVIEW:** Regulatory Affairs (RA) Business Operations believe talented people deserve a great ... and provide leadership with a clear view of progress against strategic goals. You will lead relevant communication efforts for the TAs and act as a change agent for… more
    Gilead Sciences, Inc. (08/14/25)
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