• Merck & Co. (North Wales, PA)
    …/Senior Director in the Office of Promotion and Advertising Review (OPAR)The Associate Director is responsible for the review and approval of all US ... divisions Office of Promotion and Advertising Review(OPDP)/Advertising and promotional labeling branch (APLB), including complex regulatory questions and submissions… more
    HireLifeScience (10/01/24)
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  • Associate Director , RA…

    J&J Family of Companies (Titusville, NJ)
    Associate Director , RA Labeling Product Leader (1 of 2) - 2406187352W **Description** Johnson & Johnson Innovative Medicine is recruiting for an Associate ... + Lead the development, revision, review, agreement, and maintenance of primary labeling (the Company Core Data Sheet (CCDS), United States Package Insert (USPI)… more
    J&J Family of Companies (08/10/24)
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  • Associate Director , Global…

    Takeda Pharmaceuticals (Trenton, NJ)
    …possible in order to bring life-changing therapies to patients worldwide. Join Takeda as Associate Director , Global Labeling Lead where you will be ... responsible for the development and implementation of labeling content and strategy of multiple assigned products in various stages of drug development, which may… more
    Takeda Pharmaceuticals (07/18/24)
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  • Associate Director , Regulatory…

    Ascendis Pharma (Princeton, NJ)
    …workplace for employees to grow and develop their skills. The Regulatory Affairs (RA) Associate Director , Labeling will be responsible for labeling ... States and the Americas and supporting global needs as required. The RA Associate Director , Labeling will be overall responsible for ensuring compliance with… more
    Ascendis Pharma (07/15/24)
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  • Associate Director , Advertising…

    Merck (North Wales, PA)
    …/Senior Director in the Office of Promotion and Advertising Review (OPAR) The Associate Director is responsible for the review and approval of all US ... divisions Office of Promotion and Advertising Review(OPDP)/Advertising and promotional labeling branch (APLB), including complex regulatory questions and submissions… more
    Merck (10/01/24)
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  • Associate Director , Regulatory…

    Bausch Health (Bridgewater, NJ)
    …your skills and values drive our collective progress and impact. The Associate Director , Advertising and Promotion, Prescription Drug Products, reviews, approves ... and monitors prescription drug product advertising and promotional labeling pieces for compliance with regulatory agency requirements. Responsibilities **:** +… more
    Bausch Health (09/24/24)
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  • Associate Director , US Medical…

    Bristol Myers Squibb (Princeton, NJ)
    …in their personal lives. Read more: careers.bms.com/working-with-us . **Position:** Associate Director , Medical Promotional Review Scientist, Neuropsychiatry ... **Location:** Princeton Pike, NJ or Madison, NJ The Associate Director , Medical Promotional Review Scientist plays a critical role in the Medical Strategy team.… more
    Bristol Myers Squibb (10/03/24)
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  • Associate Director , Signal…

    J&J Family of Companies (Titusville, NJ)
    Associate Director , Signal Detection Scientist - 2406212640W **Description** Johnson and Johnson is currently seeking an ** Associate Director , Signal ... event data reviews, evaluations of drug safety issues, adverse event dictionaries, core labeling , and Periodic Safety Review preparation * Ability to lead projects *… more
    J&J Family of Companies (09/19/24)
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  • Associate Director , Regulatory…

    Bristol Myers Squibb (Princeton, NJ)
    …with HA deadlines. + Contribute in the developing of target labeling . **Degree / Experience Requirements** + Bachelor's degree required; advanced scientific ... degree preferred (Masters, PhD, PharmD, BSN, etc.) with 5 years in the industry with at least 4+ years of US Medical Device Regulatory Affairs experience **Key Competencies** + Experience in successfully leading teams; ability to broadly represent the… more
    Bristol Myers Squibb (09/30/24)
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  • Associate Director , Global…

    Bristol Myers Squibb (Princeton, NJ)
    …or GRL as needed + Provide strategic direction (and content input) on US Labeling + Anticipate and interpret key trends and changes in the global/US regulatory ... environment and provide strategic guidance regarding development plans as a result. + Foster positive relationships with FDA. + Build and maintain a strong, collaborative relationship with all key stakeholders including Commercial, Medical Affairs, Promotion &… more
    Bristol Myers Squibb (09/23/24)
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  • Senior Associate , Regulatory Affairs

    J&J Family of Companies (Skillman, NJ)
    Senior Associate , Regulatory Affairs - 2407025090W **Description** Kenvue is currently recruiting for: Senior Associate , Regulatory Affairs, Dietary Supplements ... This position reports to the Director , Regulatory Affairs and is based in Skillman. **Who...**Pay: 84k- 152k** **What you will do** The Senior Associate , Regulatory Affairs is responsible for developing regulatory strategy… more
    J&J Family of Companies (09/07/24)
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  • Manager - Regulatory Affairs - Therapeutic Area

    Novo Nordisk (Princeton, NJ)
    …The Position Manage and oversee all assigned projects/products/processes. Assist the Director / Associate Director in assuring Novo Nordisk compliance ... regulatory agencies. Supervise designated personnel. Relationships Report to the Director / Associate Director /Lead Regulatory Scientist/Sr. Manager Regulatory… more
    Novo Nordisk (08/03/24)
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  • LM Critical Reagents Operations Lead

    Merck (West Point, PA)
    …through pipeline acceleration and uninterrupted supply of commercial products. The Associate Director , Large Molecule (LM) Critical Reagents (CR) Operations, ... for our company's growing inline large molecule product portfolio. The LM CR Operations, Associate Director will lead a team responsible for the execution of… more
    Merck (10/03/24)
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