• Associate Director , PV Sciences

    Taiho Oncology (Princeton, NJ)
    …guiding principles, we earn and maintain the confidence of patients, the global healthcare community, collaborators and partners, and each other. Together, we are ... Embark on a transformative journey with Taiho Oncology as an Associate Director in PV Sciences. At the forefront of pharmacovigilance innovation, we offer… more
    Taiho Oncology (11/04/25)
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  • Associate Director , Submissions Content…

    Merck (Rahway, NJ)
    …Programs, FDA Regulations, IT Coordination, IT Operation, Pharmacovigilance, Policy Implementation, Regulatory Compliance, Regulatory Labeling , Regulatory ... Source Management Business Operations Lead is expected to understand the end-to-end regulatory submission process. The main focus will be on document production… more
    Merck (12/11/25)
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  • Senior Manager, US Regulatory Affairs…

    Coty (Morris Plains, NJ)
    global ingredient policy development and defense. This position reports to the Director , NA Regulatory Affairs and R&D Material Management and is based in ... Senior Manager, US Regulatory Affairs and Ingredient Support **SENIOR MANAGER, US...retailers. + Provide guidance to Product Development regarding OTC labeling and claims. Including working with the global more
    Coty (11/10/25)
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  • Sr. Manager, Supply Chain

    Mitsubishi Chemical Group (Jersey City, NJ)
    …pharmaceutical company that has tirelessly pursued medical breakthroughs with global reach. Tanabe Pharma Corporation has discovered and produced several ... development, distribution, importation, export, and vendor management in cooperation with Director of Commercial Supply Chain. This incumbent will drive supply chain… more
    Mitsubishi Chemical Group (09/24/25)
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  • Medical Information Manager, Innovative Medicines

    Teva Pharmaceuticals (Parsippany, NJ)
    …and work closely with key members of internal departments including, Legal, Regulatory Affairs, Marketing, Global Health Economics, Value and Outcomes ( ... This review is done in collaboration with Legal and Regulatory members (PARC, Promotional Advertising Review Committee) to ensure...etc.), and coordinates review with USMA therapeutic area Medical Director , Global Medical Director , USMA… more
    Teva Pharmaceuticals (10/29/25)
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  • Program Safety Lead, GPS Medical Science

    Ascendis Pharma (Princeton, NJ)
    labeling , investigator brochures, protocols, informed consent forms, and regulatory submissions + Collaborate with internal and external stakeholders on ... patient safety and ready to help lead a fast-paced, global pharmacovigilance organization? Ascendis Pharma is seeking an experienced...role The role of Program Safety Lead is a director level position here at Ascendis and this Lead… more
    Ascendis Pharma (10/15/25)
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