• Regulatory Affairs Clinical

    Amneal Pharmaceuticals (Piscataway, NJ)
    …The Associate II (A), assists with minimal guidance, the Senior Director of Regulatory Affairs Clinical / FDA Communications.Assists the Senior ... communications/ updates Essential Functions: + Assist the Senior Director of Clinical Regulatory Affairs / FDA Communications in managing, coordinating,… more
    Amneal Pharmaceuticals (11/14/24)
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  • Director, Regulatory Affairs

    Regeneron Pharmaceuticals (Basking Ridge, NJ)
    The Director Regulatory Affairs will provide leadership on global regulatory activities for the assigned products. Responsibility will mainly focus on ... Clinical Regulatory filings and provide ...if:** + If you bring strong understanding of US FDA and international pharmaceutical guidance, regulations, drug development process,… more
    Regeneron Pharmaceuticals (12/11/24)
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  • Associate Director, Global Regulatory

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …pharmaceutical industry experience required + 4 or More Years of direct regulatory affairs experience, including US labeling experience required + Experience ... This position serves as the GRA labeling expert to the Global Regulatory Team (GRT) and independently provides strategic and operational leadership on product… more
    Daiichi Sankyo Inc. (10/19/24)
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  • Director, Global Regulatory Leader (GRL)

    J&J Family of Companies (Raritan, NJ)
    …of local labels as appropriate. + Provides regulatory input to clinical development programs, risk/benefit assessments, and medical affairs programs. + ... strategies are in alignment with product portfolio, regional strategies, CMC- Regulatory Affairs strategy, commercial and market access...+ Serve as primary point of contact for US FDA + Lead the regulatory response team… more
    J&J Family of Companies (12/10/24)
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  • Director, Clinical Operations, Specimen…

    BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
    …other relevant technical degree with minimum 10 years of leadership experience in clinical affairs . Advanced degree (eg MPH, PhD) preferred.* Previous experience ... SOCRA or ACRP credential highly preferred* Broad knowledge and experience with clinical affairs regulations and implementation.* Demonstrated track record of… more
    BD (Becton, Dickinson and Company) (11/18/24)
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  • Clinical Trials Manager, Clinical

    Gilead Sciences, Inc. (Parsippany, NJ)
    … trials, across all therapeutic areas, around the world. In partnership with Clinical Research, Medical Affairs and Development functions, ensures that all ... aspirations. Join Gilead and help create possible, together. **Job Description** ** CLINICAL OPERATIONS:** Clinical Operations is responsible for the execution… more
    Gilead Sciences, Inc. (01/09/25)
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  • Sr. Clinical Trials Manager,…

    Gilead Sciences, Inc. (Parsippany, NJ)
    …trials, across all therapeutic areas, around the world. In partnership with Clinical Research, Medical Affairs and Development Operations functions, ensures that ... aspirations. Join Gilead and help create possible, together. **Job Description** ** CLINICAL OPERATIONS:** Clinical Operations is responsible for the execution… more
    Gilead Sciences, Inc. (01/09/25)
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  • Director, Labeling

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …rare diseases and immune disorders. **Summary** This position serves as the Global Regulatory Affairs (GRA) Labeling Strategy expert to the Global Product Team ... on new product labeling in collaboration with the Global Regulatory Leads (GRLs) and Clinical Safety &...for cross-functional teams on RA labeling issues. Collaborate with Regulatory Affairs and Labeling colleagues in other… more
    Daiichi Sankyo Inc. (10/23/24)
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  • Director Labeling

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …rare diseases and immune disorders. **Summary** This position serves as the Global Regulatory Affairs (GRA) Labeling Strategy expert to the Global Product Team ... on new product labeling in collaboration with the Global Regulatory Leads (GRLs) and Clinical Safety &...for cross-functional teams on RA labeling issues. Collaborate with Regulatory Affairs and Labeling colleagues in other… more
    Daiichi Sankyo Inc. (11/20/24)
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  • Director, PV Strategic Partner Management

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …relationships with key stakeholders within CSPV and external functions including Clinical Development, Research Development, Regulatory Affairs . Facilitate ... trends, legislative changes, and guidelines issued by global regulatory agencies ( FDA , EMA, MHRA, etc.) related...and drug coding conventions (MedDRA, WHO-DD) - Knowledge of FDA and global PV regulations, clinical and… more
    Daiichi Sankyo Inc. (11/16/24)
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  • US Medical Director, Mainline Vaccines

    Sanofi Group (Morristown, NJ)
    …of medical information and clinical trial data for pharmacovigilance (PV) and regulatory reports to the US FDA and other health authorities. + Collaborate ... work in close partnership with other departments including brand teams and Public Affairs + Play a leadership role in developing, executing, and contributing to the… more
    Sanofi Group (11/18/24)
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  • Global Pharmacovigilance Audit & Inspection…

    Sanofi Group (Morristown, NJ)
    …**About you** **Experience** : + 1+ year of experience in Pharmacovigilance / Medical Affairs / Regulatory Affairs or Quality Assurance. + Experience in ... grow. We provide those opportunities in various functions such as: marketing, finance, regulatory , supply chain, clinical trials, production, etc. and in more… more
    Sanofi Group (01/11/25)
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