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company:(takeda pharmaceutical company limited)
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Assoc Director, US Ad/Promo Regulatory Review, GI (USBU) Review serves as an internal expert on FDA regulations, guidance, and enforcement trends governing the promotion of prescription drug and biologic products...
Manager, US Medical Ad/Promo Regulatory Duties: Works collaboratively with colleagues in Regulatory Affairs, Medical, Legal, Commercial, and Compliance organizations and applies Regulatory knowledge to ensure promotional and non-promotional material development..
Manager, Medical Ad/Promo Regulatory The candidate will serves as an internal resource on FDA regulations, guidance, and enforcement trends governing the promotion of prescription drug and biologic products. Will manage..
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Regulatory Labeling Strategy Lead Duties: Drives labeling strategy for the PDT BU via the development and lifecycle management of the CCDS, US, and EU labels. Formulates and implements innovative regulatory..
Lead Counsel, Brand Attorney Duties: Serve as senior legal advisor for Oncology Business Unit to appropriately execute oncology strategy and brand objectives. Lead and manage the overall legal risk assessments..
Senior Counsel IP Duties: Represent IP in and establish rapport and positive working relationships with project/program teams by acting as their advisor on a variety of IP related issues including..
Director, Federal Government Affairs Duties: Lead lobbying effort through the establishment and maintenance of professional trusted advisor relationships with Members of Congress, staff, executive branch and federal agency officials. Execute..
Lead Corporate Counsel The candidate will provide legal support and technical expertise to designated corporate functions including Global Business Development, the Center for External Innovation within R&D, Finance, Tax, Treasury..
Lead Counsel IP The candidate will provide the organization with expertise in a variety of intellectual property issues including Therapeutic Area, Region and/or Global Function support. This position, in particular,..
Team Lead, Regulatory Affairs CMC, Plasma-Derived Therapies Responsibilities: Proactively contributes to the development and implementation of innovative CMC regulatory strategies in close collaboration with relevant R&D, PDT(Plasma-Derived Therapies) BU R&D..
Associate Director, US Medical Ad/Promo Regulatory Review The candidate will understand and interpret complex issues about regulatory requirements and promotional strategy. Mentor and develop staff. Supervise, train and provide technical..
Regulatory Affairs CMC Manager, Plasma-Derived Therapies Business Unit Duties: Proactively contributes to the development and implementation of innovative CMC regulatory strategies in close collaboration with relevant R&D, PDT BU R&D..