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Collaborates closely with the US HEOR group on biologics-related activities (providing input into early economic models/endpoints, guiding trial design, assimilating HEOR input, and supporting data review for secondary publications), and presenting this back to the medical affairs teams.
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Collaborates with cross-functional teams, including sales, marketing, medical affairs, market access and policy/advocacy (MAPA), Centers of Excellence (COEs), regulatory affairs, and other relevant NNI departments to ensure alignment of consumer brand objectives and strategies, effective execution of customer experience strategies and transparent communications outside the department.
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Review incoming correspondence from the USPTO and all foreign patent offices and agents, and timely docket all due dates worldwide. Correspond with internal/outside patent counsel and foreign agents during prosecution of applications and assist with preparation of prosecution papers such as responses to office actions and information disclosure statements.
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Biotech / Pharmaceutical industry experience, with strong understanding of solid tumor drug development and medical affairs function. Reporting to the Global Medical Affairs Strategy Lead (MASL) the Director will be responsible for the development and execution of the Global Medical Affairs strategic and tactical plans for the asset(s) for the primary indication as well as new indications to expand into as part of the asset life cycle management.
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Experience working with legal counsel on regulatory and legislative affairs. The Virtual Power Plant Policy Director will lead SUN’s policy, regulatory, and advocacy efforts to implement solar + batteries Virtual Power Plant (VPP) policy across the country and in targeted states.
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With 5 years in the industry with at least 4+ years of US Medical Device Regulatory Affairs experience. Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
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Candidate must be a U.S. Citizen or national, permanent resident, refugee or asylee, or temporary resident under the legalization program of the 1986 Immigration Act. Sunny Delight Beverages Company does not offer practical training positions nor sponsor foreign citizens to obtain work visa or permanent residency (except for certain highly specialized roles such as some R&D positions requiring Doctorate degrees.
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Lead annual medical planning for asset(s) ; Work closely with extended medical affairs functions (global and regional markets) to inform and implement overall medical strategy for designated products and/or therapeutic areas.
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5-7 years of pharmaceutical and or life sciences marketing experience; additional pharmaceutical experience in sales, medical affairs, and market access a plus Experience with marketing and/or selling biologics within at least two of the following disease areas is REQUIRED : dermatology, immunology, rheumatology.
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The Director, Corporate Counsel – Rare Disease will serve as the legal advisor to the US Commercial, Patient Advocacy, Public Affairs, Regulatory, and Medical Affairs teams supporting our Rare Disease Franchise, and will coordinate legal services with the attorney responsible for Canadian support for the Rare Disease Franchise.
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Collaborate with the International Tax Director on Subpart F, GILTI, FDII, Sec. 163(j), BEAT, foreign tax credit, and other international items included on the US Consolidated Tax Return. Build and maintain effective relationships with Tax Planning, Tax Reporting, Tax Technology, Transfer Pricing, Tax Disputes, and the Controller’s Group.
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S/he will report to the Executive Director and is a key business partner for Immunology & Neuroscience Medical Affairs. The Senior Director, Medical Performance and Outcomes (MPO) will support the MPO capability globally to drive the value of Immunology & Neuroscience Medical Affairs.
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Their responsibilities include: Collecting, analyzing and exploiting foreign language communications of interest Transcribing, translating and interpreting foreign language materials Providing cultural and regional guidance in support of Navy, Joint Force, national and multinational needs Cryptologic Technician Technical (CTT) - CTTs serve as experts in airborne, shipborne and land-based radar signals.
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It is Siemens Healthineers’ policy to comply fully and completely with all United States export control laws and regulations, including those implemented by the Department of Commerce through the Export Administration Regulations (EAR), by the Department of State through the International Traffic in Arms Regulations (ITAR), and by the Treasury Department through the Office of Foreign Assets Control (OFAC) sanctions regulations.
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You will join a global team of quality analysts who support a multilingual research team in researching, recording and updating details on individuals and entities mentioned in Sanctions & Other Official Lists (Special Lists) issued by government bodies and regulators around the world, for example, the Office of Foreign Assets Control in the US, national law enforcement bodies or securities regulators.
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foreign affairs jobs Title: data Company: Abbott Laboratories in Princeton, NJ
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