• Merck & Co. (North Wales, PA)
    Job DescriptionPosition Description: Legal Director ( FDA promotion /Labeling Drugs & Vaccines) The position provides legal support to the Human Health ... a focus on counseling clients in the areas of FDA promotion and labeling of drugs and...labeling of drugs and vaccines.- The position also provides legal support to the Research Division and Compliance department… more
    HireLifeScience (05/09/24)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    …knowledge and understanding of the Anti-kickback Statute, the False Claims Act, FDA rules and regulations regarding the promotion of pharmaceuticals, government ... the highest ethical & privacy standards and ensuring adherence to corporate and legal regulations, this team is constantly called upon to design and implement… more
    HireLifeScience (04/20/24)
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  • Legal Director ( FDA

    Merck (North Wales, PA)
    **Job Description** **Position Description:** ** Legal Director ( FDA promotion /Labeling Drugs & Vaccines)** The position provides legal support to the ... a focus on counseling clients in the areas of FDA promotion and labeling of drugs and...labeling of drugs and vaccines. The position also provides legal support to the Research Division and Compliance department… more
    Merck (05/09/24)
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  • Associate Director , US Advertising…

    Sanofi Group (Cambridge, MA)
    About the Role The Associate Director , US Regulatory Affairs (RA) serves as the regulatory lead on relative Review Committees (RCs), for products in the Rare ... competitively positioning assigned products appropriately while maintaining compliance with applicable FDA regulations and company policies for the advertising and … more
    Sanofi Group (03/21/24)
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  • Associate Director , Regulatory Affairs…

    Astellas Pharma (Northbrook, IL)
    …and external business partners. + Effectively applies strong working knowledge of FDA guidance and promotion standards to business situations and medical ... the requirements for promotional materials as set forth by FDA . Advises teams on best practices regarding planning and...development. **Organizational Context:** Position will report to a Sr Director or Director of Promotion more
    Astellas Pharma (05/14/24)
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  • Associate Director , US Advertising…

    Sanofi Group (Bridgewater, NJ)
    The Associate Director RA serves as the regulatory lead on Review Committees (RCs). As the RC RA representative, work with brands on competitively positioning ... assigned products appropriately while maintaining compliance with applicable FDA regulations, company policies, and applicable Industry Guidelines for the… more
    Sanofi Group (03/21/24)
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  • Associate Director - Regulatory Affairs…

    Novo Nordisk (Princeton, NJ)
    …a living. Are you ready to make a difference? The Position The Associate Director , Regulatory Affairs - Advertising & Promotion will provide strategic regulatory ... positive working relationship with OPDP reviewers. Report to Senior Director , Regulatory Affairs - Advertising & Promotion ....concepts that meet business objectives + Provide training in FDA regulations for advertising and promotion to… more
    Novo Nordisk (05/09/24)
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  • Senior Director , Commercial Regulatory…

    Mitsubishi Chemical Group (Jersey City, NJ)
    …real-world evidence, and creating hope for all facing illness. The Senior Director , Commercial Regulatory Affairs, is responsible for the development and execution ... submissions, regulatory compliance, regulatory advice and counseling, advertising and promotion reviews, and marketing application registration updates in close… more
    Mitsubishi Chemical Group (03/01/24)
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  • Associate Director , US Medical Advertising…

    Takeda Pharmaceuticals (Lexington, MA)
    …expert on FDA regulations, guidance, and enforcement trends governing the promotion of prescription drug and biologic products. You will be able to provide ... expert on FDA regulations, guidance, and enforcement trends governing the promotion of prescription drug and biologic products. The role thoroughly reviews and… more
    Takeda Pharmaceuticals (05/11/24)
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  • Associate Director , Consumer Marketing…

    Bristol Myers Squibb (Princeton, NJ)
    FDA regulations and guidelines related to schizophrenia treatment promotion . **Qualifications & Experience** + Bachelor's degree in marketing, Business ... and spirit of independence and love of challenge. **Title** : Associate Director , Consumer Marketing - Schizophrenia **Position Summary:** We are seeking an… more
    Bristol Myers Squibb (05/15/24)
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  • Sr. Director , Counsel-Lilly Value…

    Lilly (IN)
    …who are determined to make life better for people around the world. As Sr. Director , Counsel for Lilly Value and Access (LVA), you will join the team of attorneys ... in the US This role will work closely with others on the LVA legal team, as well cross-functionally with other attorneys, including those in brand, medical, and… more
    Lilly (05/12/24)
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  • Director , Research Contracts -…

    Houston Methodist (Houston, TX)
    …the Houston Methodist Academic Institute and Houston Methodist Department of Legal Services. The Director position responsibilities include overseeing the ... At Houston Methodist, the Director , Research Contracts position is responsible for providing...strategic support for research activities and acts as a legal expert and liaison between all department personnel and… more
    Houston Methodist (04/16/24)
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  • Director , Agile Sourcing, Enabling…

    Bristol Myers Squibb (Princeton, NJ)
    …at work and in their personal lives. Read more: careers.bms.com/working-with-us . The Director of Agile Sourcing - Enabling Services (ES) focused position plays a ... terms are translated into contractual terms, following BMS templates provided by Legal Dept / Strategic Corporate Transactions, and working in close partnership with… more
    Bristol Myers Squibb (05/06/24)
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  • Associate Director - CMC Program Management

    Lilly (Indianapolis, IN)
    …to make life better for people around the world. **Associate Director ** **; CMC, Device Development Program Manager** **Functional Area: Technical Operations** ... million people worldwide have disabling hearing loss, and there are no FDA -approved pharmacologic therapies to address its underlying causes. Akouos was founded in… more
    Lilly (04/24/24)
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  • Senior Manager, US Medical Advertising…

    Takeda Pharmaceuticals (Lexington, MA)
    …expert on FDA regulations, guidance, and enforcement trends governing the promotion of prescription drug and biologic products. You will also provide regulatory ... the US Medical team, you will report to the Director , Ad/Promo Regulatory Review. You will be based in...FDA regulations, guidance, and enforcement trends governing the promotion of prescription drug and biologic products. Thoroughly review… more
    Takeda Pharmaceuticals (05/11/24)
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  • Senior Manager, US Medical Ad/Promo Regulatory…

    Takeda Pharmaceuticals (Lexington, MA)
    …expert on FDA regulations, guidance, and enforcement trends governing the promotion of prescription drug and biologic products. You will also provide regulatory ... on FDA regulations, guidance, and enforcement trends governing the promotion of prescription drug and biologic products. Thoroughly review and assess proposed… more
    Takeda Pharmaceuticals (03/21/24)
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  • AD or Sr. AD Corporate Counsel Life Science…

    Boehringer Ingelheim (Ridgefield, CT)
    **Description** As Associate Director , Corporate Counsel or Sr. Associate Director , Senior Counsel, you will play a pivotal role in supporting Boehringer ... Medicine, R&D and selected therapeutic areas. You will provide strategic advice and legal counsel on various regulatory legal issues including marketing and… more
    Boehringer Ingelheim (04/26/24)
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  • Clinical Research Coordinator II Non-RN

    AdventHealth (Denver, CO)
    …in accordance with trial protocols, Food and Drug Administration ( FDA ) regulations and International Conference on Harmonization/Good Clinical Practices (ICH/GCP) ... Principal Investigator (PI) oversight by advising the PI, sub-investigator(s), Lead and Director of deviations in conduct, patient status, issues relevant to the… more
    AdventHealth (05/15/24)
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  • Clinical Research Coordinator II

    AdventHealth (Orlando, FL)
    …in accordance with trial protocols, Food and Drug Administration ( FDA ) regulations and International Conference on Harmonization/Good Clinical Practices (ICH/GCP) ... Principal Investigator (PI) oversight by advising the PI, sub-investigator(s), Lead and Director of deviations in conduct, patient status, issues relevant to the… more
    AdventHealth (05/11/24)
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  • Clinical Research Coordinator II -RN

    AdventHealth (Orlando, FL)
    …in accordance with trial protocols, Food and Drug Administration ( FDA ) regulations and International Conference on Harmonization/Good Clinical Practices (ICH/GCP) ... Principal Investigator (PI) oversight by advising the PI, sub-investigator(s), Lead and Director of deviations in conduct, patient status, issues relevant to the… more
    AdventHealth (05/11/24)
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