• Merck & Co. (Rahway, NJ)
    Job DescriptionPosition Description: Senior Specialist , Clinical Literature MonitoringProvides pertinent and timely information on our Company's products and ... interests from the world's biomedical literature in support of regulatory , clinical research, marketing, and legal functions.- Plans, organizes, monitors,… more
    HireLifeScience (06/08/24)
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  • Merck & Co. (Rahway, NJ)
    …dedicated colleagues while developing and expanding your career.The Senior Trial Initiation Specialist in Global Site Budgets and Payments will be responsible for ... and presentation skills.Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines which includes knowledge of Standard of Care/Routine Care and… more
    HireLifeScience (06/08/24)
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  • Merck & Co. (Rahway, NJ)
    …CCDS, CCPPI, CCIFU) and US labeling for marketed products; and supporting country Regulatory Affairs in the development and maintenance of the EU Labeling and other ... and implementing US Labeling for assigned products in line with regulatory requirements and internal standards and guidelines.- Assisting with developing and… more
    HireLifeScience (06/07/24)
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  • Merck & Co. (Rahway, NJ)
    …Pharmacology and Pharmacometrics --Immune/Oncology-(QP2-IO)-team in the role of-Senior Specialist .--QP2-IO team is part of the Global Clinical Development ... senior scientists you will develop a comprehensive understanding of global regulatory expectations for small molecules and biologics, including support and authoring… more
    HireLifeScience (06/04/24)
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  • Eisai, Inc (Nutley, NJ)
    …mild cognitive impairment due to Alzheimer's disease (AD) or mild AD. TheNeurology Account Specialist (NAS) will be part of a diverse team of sales professionals who ... sales/business analytics, etc.)Strong understanding of pharmaceutical manufacturer compliance & regulatory requirementsDemonstrated success in driving growth and profitability, establishing… more
    HireLifeScience (05/28/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …global function on study and project teamsProduces independent writing for publications and regulatory documentsServes as a specialist in PK-PD and Pop PK-PD ... function on study and project teams, and participate in and contribute to regulatory and KOL meetings. This position requires significant understanding of PK-PD and… more
    HireLifeScience (05/01/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …global function on study and project teamsProduces independent writing for publications & regulatory documentsServes as a specialist in PK-PD and Pop PK-PD ... hands on population PK and PKPD analyses and participate in regulatory interactions and submissions representing the Clinical Pharmacology and Pharmacometrics/… more
    HireLifeScience (04/23/24)
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  • Legend Biotech USA, Inc. (Raritan, NJ)
    …treatment of multiple myeloma. Legend Biotech is seeking a Master Data Governance Sr. Specialist as part of the Technical Operations team based in Raritan, NJ. Role ... Overview We are actively seeking a proficient SAP Master Data Sr. Specialist with a specific focus on Materials orchestration throughout the End-to-End Manufacturing… more
    HireLifeScience (06/04/24)
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  • Legend Biotech USA, Inc. (Raritan, NJ)
    …of an immunotherapy in the treatment of multiple myeloma. Legend Biotech is seeking QC Specialist , Lab Services - I, II, III as part of the Quality team based in ... Raritan, NJ. Role Overview The QC Specialist , Lab Services, is responsible for sample management. The...handle corrective and preventative action records. Supports internal and regulatory audits. Requirements A minimum of a Bachelor's degree… more
    HireLifeScience (03/28/24)
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  • Legend Biotech USA, Inc. (Raritan, NJ)
    …of multiple myeloma. Legend Biotech is seeking a QA Warehouse Incoming Raw Material Specialist as part of the Quality team based in Raritan, NJ. Role Overview The ... QA Warehouse Incoming/Raw Material Specialist is an exempt level position with responsibility to be part of the team responsible for Warehouse activities that will… more
    HireLifeScience (03/13/24)
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  • Senior Regulatory Specialist

    Hackensack Meridian Health (Hackensack, NJ)
    …transform healthcare and serve as a leader of positive change. The **Senior Regulatory Specialist ** is responsible for the oversight and management of clinical ... clinical trials. **Responsibilities** A day in the life of a **Senior Regulatory Specialist ** at **Hackensack Meridian** **_Health_** includes: + Assists with… more
    Hackensack Meridian Health (05/18/24)
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  • Regulatory Specialist

    Hackensack Meridian Health (Hackensack, NJ)
    …to transform healthcare and serve as a leader of positive change. The ** Regulatory Specialist ** is responsible for ensuring compliance with Federal, State, and ... assigned clinical trials. **Responsibilities** A day in the life of a ** Regulatory Specialist ** at **Hackensack Meridian** **_Health_** includes: + Organizes and… more
    Hackensack Meridian Health (05/21/24)
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  • Regulatory Specialist

    Eaton Corporation (Long Branch, NJ)
    Eaton's ES EMEA CS LS division is currently seeking a Regulatory Specialist . This role is based out of our Sarasota, FL OR Long Branch, NJ facilities. The ... Regulatory Specialist will be responsible for developing, maintaining, and executing product certifications for new and existing products. This individual will… more
    Eaton Corporation (05/02/24)
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  • Regulatory Affairs Specialist --Home…

    RELX INC (New York, NY)
    Regulatory Affairs Specialist About the Team LexisNexis Reed Tech serve manufacturers and distributors of medical devices and drug products, and those who ... world. About the Role We are seeking a versatile and strategic Regulatory Affairs Specialist to join our dynamic Reed Tech Life Sciences Professional Services.… more
    RELX INC (05/17/24)
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  • Senior Staff Regulatory Affairs…

    Stryker (Allendale, NJ)
    …is available at www.stryker.com We are currently seeking a **Senior Staff Regulatory Affairs Specialist ** to join our **Spine Division** based **Hybrid** ... regulations and expectations. **What you will do** As the Senior Staff Regulatory Affairs Specialist , you will work to maintain medical devices on the market and… more
    Stryker (05/23/24)
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  • Regulatory Affairs Specialist

    BPL Plasma (Fort Lee, NJ)
    **Position** : Regulatory Affairs Specialist **Location** : Fort Lee, NJ **Duties and Responsibilities:** 1. Ensures Regulatory compliance within KEDPLASMA ... Operating Procedures and other applicable Standards and Protocols to meet the regulatory requirements of the FDA, EMEA, Customer Specifications, and other … more
    BPL Plasma (05/30/24)
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  • Staff Regulatory Affairs Specialist

    BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
    **Job Description Summary** The Staff Regulatory Affairs Specialist will work in BD Medical - Pharmaceutical Systems Business Unit taking on a lead role at the ... project level in developing and executing regulatory strategy and compliance plans to promote and support drug delivery solutions for pharma combination product… more
    BD (Becton, Dickinson and Company) (05/30/24)
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  • Senior Staff Regulatory Compliance…

    Stryker (Mahwah, NJ)
    …organization by visiting stryker.com We are currently seeking a **Senior Staff Regulatory Compliance Specialist ** to join our Joint Replacement Division based ... and expectations. **What you will do** As **Senior Staff Regulatory Compliance Specialist ** , you will support organizational decision on product field… more
    Stryker (06/07/24)
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  • Regulatory Affairs Specialist

    Kelly Services (Bridgewater, NJ)
    ** Regulatory Affairs Specialist (Hybrid)** Kelly(R) Science & Clinical is seeking a Regulatory Affairs Specialist for our client in Bridgewater, New ... into 2024 **Pay:** $43.00-45.00 an hour + **Responsibilities** **:** Provide Regulatory Documentation Support to Global RA team members for Product Registrations,… more
    Kelly Services (06/08/24)
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  • Program, Policy, and Domestic Violence…

    City of New York (New York, NY)
    …Services NM II, to function as a Program, Policy, and Domestic Violence Regulatory Compliance Specialist who will: Under administrative direction of the ... matters as directed for submission to Commissioner, governmental and non-governmental regulatory bodies. - Manage all DV special projects, special inquiries, and… more
    City of New York (04/30/24)
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