• Merck & Co. (Rahway, NJ)
    …keeping up with the latest regulatory guidelines and trends.Collaborate with global regulatory teams to align strategies and ensure submission readiness in ... Job DescriptionThe Executive Director , Device Quality & Regulatory will...emerging regulations and industry trends affecting device quality and regulatory affairs .Strategic ContributionsServe as a key member… more
    HireLifeScience (11/09/24)
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  • Merck & Co. (Rahway, NJ)
    …Work effectively with cross-functional partners including research and development, medical affairs , regulatory affairs , manufacturing, Business Development ... competitive strategy, target product profile development, health authority interactions, global regulatory filing strategy, launch readiness reviews, organized… more
    HireLifeScience (11/06/24)
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  • Merck & Co. (Rahway, NJ)
    …Experience and Skills:Minimum 10 years' experience in communications and corporate affairs ; healthcare and pharmaceutical experience at global publicly-traded ... Job DescriptionThe Executive Director , Vaccines Communications is responsible for leading, developing...is responsible for leading, developing and executing US and global communications strategies and programs that support our Company's… more
    HireLifeScience (11/09/24)
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  • Merck & Co. (Rahway, NJ)
    …studiesWork closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical ... Job DescriptionOur company is a global health care leader with a diversified portfolio...of clinical development, including study design, placement, monitoring, analysis, regulatory reporting, and publication.Specifically, the Senior Director more
    HireLifeScience (11/16/24)
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  • Merck & Co. (Rahway, NJ)
    …studies;Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical ... Job DescriptionOur company is a global health care leader with a diversified portfolio...of clinical development, including: study design, placement, monitoring, analysis, regulatory reporting, and publication.Specifically, the Director may… more
    HireLifeScience (11/13/24)
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  • Director , Regulatory Affairs

    AbbVie (Florham Park, NJ)
    …Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description The Director Regulatory Affairs , Strategic Labeling is responsible for ... and product labeling (CCDS, US/EU labeling documents) at Senior level meetings ( Global Regulatory Forum (GRF), Executive Labeling Committee (ELC), Steering… more
    AbbVie (09/20/24)
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  • Associate Director of Regulatory

    Insight Global (Florham Park, NJ)
    Job Description Insight Global is seeking an Associate Director of Regulatory Affairs to join the one of our pharmaceutical clients in Florham Park, NJ. ... This position is responsible for developing and executing regional regulatory strategies for antiviral products. It is essential that this person has experience… more
    Insight Global (11/05/24)
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  • Director , Regulatory Affairs

    Mitsubishi Chemical Group (Jersey City, NJ)
    …on real-world evidence, and creating hope for all facing illness. The Director , Regulatory Affairs provides strategic global regulatory guidance to ... and guidelines. + Leads as a key member of Global Regulatory Project Teams. + Leads multidisciplinary...requests, and briefing documents. + Acts as liaison between Regulatory Affairs and other functional areas, including… more
    Mitsubishi Chemical Group (10/18/24)
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  • Director , Regulatory Affairs

    Merck (Rahway, NJ)
    …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 (11/09/24)
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  • Associate Director , Regulatory

    Gilead Sciences, Inc. (Parsippany, NJ)
    Regulatory Advertising and Promotion (RA Ad/Promo) is a core function within Gilead's Global Regulatory Affairs organization and acts as a critical ... or other special projects. May initiate and/or contribute to global process improvements. + Provides regulatory guidance...Experience working with external contractors supporting the work of regulatory affairs is a plus. + Experience… more
    Gilead Sciences, Inc. (11/16/24)
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  • Medical Director /Scientific…

    AbbVie (Florham Park, NJ)
    …with the scientific review, development, approval, execution, and communication of affiliate/area/ global medical affairs sponsored or supported clinical research ... the regulatory requirements related to the clinical studies and global drug development and accountable for complying with those requirements. + Responsible… more
    AbbVie (09/26/24)
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  • Medical/Scientific Director , Medical…

    AbbVie (Florham Park, NJ)
    …understanding of relevant therapeutic area required. + 7-10 years of experience in Medical Affairs with Global Medical Affairs experience highly preferred. + ... and scientific strategic and operational input into core medical affairs activities such as: healthcare professional/provider interactions (HCPs, Patients and… more
    AbbVie (09/20/24)
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  • Associate Director , US Medical…

    Bristol Myers Squibb (Madison, NJ)
    …as appropriate. **Key Responsibilities** + Support development and execution of the US Medical Affairs plans, in coordination with the Global Medical Affairs ... work and in their personal lives. Read more: careers.bms.com/working-with-us . The Associate Director , US Medical, Multiple Myeloma will report to the Director ,… more
    Bristol Myers Squibb (11/17/24)
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  • Regional Associate Director , Medical…

    Merck (Rahway, NJ)
    …medicines that help people with cancer across the globe. The Regional Associate Director of Medical Affairs - Gastrointestinal Cancer (RADMA) position is a ... with the Upper GI and Lower GI US Regional Director of Medical Affairs (RDMAs) and partner...to provide region-specific strategic input into the development of global medical affairs plans + Collaborates across… more
    Merck (11/12/24)
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  • Associate Medical/Scientific Director

    AbbVie (Florham Park, NJ)
    …statistics, regulatory , etc.) as they relate to on-going medical affairs projects. + Experience in Neuroscience/Psychiatry preferred. + May assist as consultant ... be determined by the qualifications listed below. Purpose The Associate Scientific Director provides medical and scientific strategic and operational input into core… more
    AbbVie (10/19/24)
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  • Sr Manager Regulatory Affairs

    System One (Florham Park, NJ)
    Senior Manager, Regulatory Affairs (BRANDED PRODUCTS) Must be local for Florham Park, NJ (Hybrid 2-3 days onsite) 12-month contract (renewable) Overview The ... Contractor - Senior Manager, Regulatory Affairs - Quality of Life (QOL),...meetings related to QOL initiatives. + Support coordination with global regulatory counterparts to ensure alignment of… more
    System One (09/05/24)
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  • Associate Director , Legal Counsel, Legal…

    Scotiabank (New York, NY)
    Associate Director , Legal Counsel, Legal and Corporate Affairs **Requisition ID:** 206757 **Salary Range:** 180,000.00 - 211,800.00 _Please note that the Salary ... committed to results, in an inclusive and high-performing culture. ** Global Banking and Markets** Global Banking and...front office and other internal stakeholders on legal and regulatory matters related to the business. + Independently draft… more
    Scotiabank (11/12/24)
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  • Associate Principal Scientist, Regulatory

    Organon & Co. (Jersey City, NJ)
    …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 Principal Scientist, Regulatory

    Organon & Co. (Jersey City, NJ)
    …agile manner. + Provide Regulatory CMC and oversight in developing global Regulatory CMC strategies and executing submissions related to diverse late-stage ... Position** Reporting to the Director or Executive Director in Organon Regulatory CMC New Products,...participating in Agency meetings on CMC topics, and executing global initial marketing applications with a line of sight… more
    Organon & Co. (10/08/24)
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  • Senior Scientist, Regulatory Affairs

    Organon & Co. (Jersey City, NJ)
    regulatory strategies by performing assessments of CMC changes, identifying global regulatory requirements, and critically evaluating supporting documentation ... **Job Description** **The Position** Reporting to the Director in Regulatory Chemistry, Manufacturing and...to assess acceptability and identify potential risks. + Execute global regulatory strategies by leading the development,… more
    Organon & Co. (11/13/24)
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