• Associate Director , Global

    CSL Behring (King Of Prussia, PA)
    …biotherapies used to treat serious and often rare conditions. Could you be our next Associate Director , Global Regulatory Affairs ? The job is located in ... is a hybrid position. You will report to the Director of Global Regulatory Affairs . **Responsibilities:** You are a member of a Regional Therapeutic Area… more
    CSL Behring (12/03/24)
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  • Associate Director , Global

    Takeda Pharmaceuticals (Trenton, NJ)
    …activities pertaining to global and local labeling compliance and quality within Global Regulatory Affairs . + Partners with internal stakeholders and ... to the best of my knowledge. **Job Description** The Regulatory Affairs -Labeling, Associate Director is...external CRO partners such as Global Regulatory Compliance, Global Labeling,… more
    Takeda Pharmaceuticals (11/27/24)
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  • Director Global Regulatory

    Takeda Pharmaceuticals (Trenton, NJ)
    …understands probabilities of technical success for the solutions. + Effectively represent the Global Regulatory Affairs (GRA) function in senior level ... for providing strategic guidance and oversight for the delivery of global regulatory strategies to support development of biomarkers, diagnostic tests, devices… more
    Takeda Pharmaceuticals (12/06/24)
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  • Associate Director , Regulatory

    Sumitomo Pharma (Trenton, NJ)
    Regulatory Affairs ** . The Associate Director is part of the Global Regulatory Affairs (GRA) team based in the US. He/she will primarily function ... registration strategy of a project in collaboration with the Global Regulatory Leader (GRL). He/she is expected...pharmaceutical industry with minimum of 6 years focused in Regulatory Affairs + Include the qualifications preferred… more
    Sumitomo Pharma (11/21/24)
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  • Director , Regulatory Affairs

    Sumitomo Pharma (Trenton, NJ)
    Regulatory Affairs ** . The Director is part of the Global Regulatory Affairs (GRA) team based in the US. He/she will primarily function ... as the Regional Regulatory Leader (RRL) and/or Global ...pharmaceutical industry with minimum of 8 years focused in regulatory affairs . + Master's degree required (preferably… more
    Sumitomo Pharma (11/28/24)
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  • Director , Regulatory Affairs

    Merck (North Wales, PA)
    …accountable, global regulatory point of contact on those projects within Global Regulatory Affairs and Clinical Safety (GRACS) and external to GRACS. ... release from our company to external agencies and investigators. + Represents Global Regulatory Affairs (GR) within internal committees to provide … more
    Merck (12/04/24)
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  • Global Medical Affairs Leader,…

    J&J Family of Companies (Horsham, PA)
    Johnson & Johnson is recruiting for a Global Medical Affairs Leader (GMAL), Director - Dermatology in our Immunology Global Medical Affairs ... potential. At Johnson & Johnson, we all belong. The Global Medical Affairs Leader (GMAL), Director...Excellent knowledge of study execution, benefit risk management and regulatory affairs highly preferred + Proven ability… more
    J&J Family of Companies (12/11/24)
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  • Global Medical Affairs Leader,…

    J&J Family of Companies (Horsham, PA)
    Johnson and Johnson is recruiting for a Global Medical Affairs Leader (GMAL), Director - Gastroenterology within our Global Immunology Medical Affairs ... GMAL - Gastroenterology (GI), under direction of the Head Global Immunology Medical Affairs - Gastroenterology, is...execution, data analysis & review, benefit risk management and regulatory affairs is highly preferred + Highly… more
    J&J Family of Companies (12/11/24)
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  • Associate Director , Regulatory

    Merck (West Point, PA)
    …Discovery, Preclinical and Translational Medicine Operations (DPTM) is seeking an Associate Director to lead the Molecular lab within the Late Development (AdVAnce) ... utilized to generate pivotal safety and efficacy clinical patient data required for regulatory filings. As the AdVAnce facility will not be fully constructed and… more
    Merck (12/12/24)
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  • Director , Medical Affairs Strategy…

    Sumitomo Pharma (Trenton, NJ)
    …website https://www.us.sumitomo-pharma.com or follow us on LinkedIn. **Job Overview** The Director , Medical Affairs Strategy (Hematology/Oncology) will be a key ... Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key...member of the Medical Affairs team reporting to the Executive Director ,… more
    Sumitomo Pharma (11/27/24)
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  • Senior Director , Medical Affairs

    Sumitomo Pharma (Trenton, NJ)
    Director , Medical Strategy (Rare Disease) will be a key member of the Medical Affairs team reporting to the Executive Director , Medical Affairs Strategy. ... Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key...and external facing HCP and Payer interactions. The Sr. Director of Medical Affairs develops and maintains… more
    Sumitomo Pharma (11/21/24)
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  • Director , Medical Affairs Strategy…

    Sumitomo Pharma (Trenton, NJ)
    …, Medical Strategy (Prostate Cancer)** will be a key member of the Medical Affairs team reporting to the Executive Director , Medical Affairs Strategy. ... Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key...and advance patient advocacy efforts to ensure that Medical Affairs activities align with patient focused programs. **Job Duties… more
    Sumitomo Pharma (12/05/24)
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  • Associate Director , Field Medical…

    Sumitomo Pharma (Trenton, NJ)
    …. **Job Overview** Associate Director , Field Medical and Scientific ... Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key...key insights obtained from the RDs to the Medical Affairs and other internal stakeholders in a timely manner.… more
    Sumitomo Pharma (12/14/24)
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  • Associate Principal Scientist, Regulatory

    Organon & Co. (Plymouth Meeting, PA)
    …agile manner. + Provide Regulatory CMC and oversight in developing global Regulatory CMC strategies and executing submissions related to diverse late-stage ... high-quality CMC documentation for Health Authority submissions, establishing and applying CMC global regulatory strategies, current regulatory trends and… more
    Organon & Co. (11/12/24)
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  • Associate Director , Global

    Takeda Pharmaceuticals (Trenton, NJ)
    Regulatory Project Management and Strategic Planning - GI2 TAU within our Global Regulatory Affairs organization, based remotely. + Partners with the ... implementing process changes through proactive engagements with cross functional team members, Global Regulatory Affairs TAU colleagues and Global more
    Takeda Pharmaceuticals (10/24/24)
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  • Senior Director Regulatory Group…

    CSL Behring (King Of Prussia, PA)
    Regulatory TA Head. You will play an important leadership role as part of the Global Regulatory Affairs (GRA) GPS Leadership Team. You will lead the ... often rare conditions Could you be our next Senior Director , Regulatory Lead-Enabling Healthcare Technologies? The job...Strategy Team (PST), Clinical Development Team (CDT), and within Global Regulatory Affairs (GRA). **Experience**… more
    CSL Behring (12/12/24)
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  • Senior Principal Scientist, Regulatory

    Merck (North Wales, PA)
    …Product Development Teams and regulatory single point-of-contact for products within Global Regulatory Affairs and Clinical Safety (GRACS) and external ... **Summary, Focus and Purpose** The Senior Principal Scientist | Regulatory Affairs Liaison is responsible for development...product labeling and obtain shortest time to approval by global regulatory agencies. You will independently manage… more
    Merck (12/13/24)
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  • Executive Director , Device Quality…

    Merck (Trenton, NJ)
    …up with the latest regulatory guidelines and trends. + Collaborate with global regulatory teams to align strategies and ensure submission readiness in all ... **Job Description** The Executive Director , Device Quality & Regulatory will...emerging regulations and industry trends affecting device quality and regulatory affairs . Strategic Contributions + Serve as… more
    Merck (12/06/24)
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  • Associate Director , Global Labeling…

    Takeda Pharmaceuticals (Trenton, NJ)
    …+ Appropriately escalates issues to Global Labeling management and the Global Regulatory Lead (GRL) and proposes risk mitigation strategies for assigned ... life-changing therapies to patients worldwide. Join Takeda as Associate Director , Global Labeling Lead where you will...+ Working within Labeling Team and GRA + Represents Global Labeling at Global Regulatory more
    Takeda Pharmaceuticals (10/16/24)
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  • Associate Director , Global Patient…

    Takeda Pharmaceuticals (Trenton, NJ)
    …Liaise with and advise study teams including Clinical Science, Data Management, Regulatory Affairs , and other functional areas locally/globally on matters ... of clinical trial and Pharmacovigilance methodologies including detailed comprehension of global regulatory requirements. + Good cross-cultural understanding and… more
    Takeda Pharmaceuticals (12/06/24)
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