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Supporting the Director of Global Scientific Affairs, in conjunction with the Sr. Manager and Project Manager in Global Scientific Affairs, with KOL management as it relates to investigator-sponsored studies (ISS) and/or collaborative research studies (CRS.
$286,700 a yearFull-timeExpandApply NowActive JobUpdated 2 months ago - UpvoteDownvoteShare Job
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As a Legal and Compliance Intern, you will work closely with the Legal and Compliance teams supporting business functions which may include Marketing, Sales, Medical Affairs, Market Access, Digital, HR, IT, Public Affairs, Finance, Commercial Operations, Supply Chain Management and Operations, Quality and Regulatory.
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Sales Clinical Training:Work with the Head of Scientific Affairs and the Sales Directors to identify and address training needs to improve the team's clinical knowledge. Scientific Collaborations:Collaborate with key opinion leaders under the leadership of the North America Head of Medical Affairs to engage in important discussions related to medical/clinical, health economics, and outcomes research.
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Business leaders (e.g., VP Medical Affairs, VP Regulatory Affairs, GM Genmab US, IT Lead in Japan) The focus of this role will include stakeholders in the business domains Field Operations, Medical & Regulatory Affairs and US and Japan Market and Commercial Teams (and others) and requires having a detailed and thorough understanding of the underlying operational and commercial business processes.
$275,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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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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Advise the Vice Provost for International Affairs and other University leaders on emerging andor urgent threats and risks to University interests stemming from geopolitical or other safety and security developments in the United States and abroad.
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Associate Director, CMC Regulatory Affairs. The CMC Regulatory Associate Director, Biologics is responsible for content development, compilation, maintenance, and review of the Quality Module for regulatory submissions to support biologics products regarding: Clinical trial applications; New marketing applications; HA responses & background packages (including participating/leading HA meetings); and/or post-approval submissions.
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At Genmab, we're committed to building extra[not]ordinary futures together, by developing antibody products and pioneering, knock-your-socks-off therapies that change the lives of patients and the future of cancer treatment and serious diseases.
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Johnson & Johnson Innovative Medicine is searching for an Associate Director, AI for Medical Data and Advanced Analytics to drive the data and advanced analytics roadmap for medical affairs solutions across the Neuroscience and Immunology therapeutic areas.
$232,300 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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At Genmab, we’re committed to building extra[not]ordinary futures together, by developing antibody products and pioneering, knock-your-socks-off therapies that change the lives of patients and the future of cancer treatment and serious diseases.
$159,375 a yearFull-timeExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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Collaborates with cross-functional teams, including Feld Sales, Marketing, Strategic Partnership and Engagement, Medical Affairs, Market Access and Public Affairs (MAPA), Portfolio Strategy, Commercial Excellence, Regulatory Affairs, and other relevant NNI departments to ensure alignment of therapy area objectives and strategies.
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Represent Regulatory CMC on cross-functional development/commercial teams and Regulatory Affairs teams. Participate in the development of the CMC regulatory strategy for biologics submissions.
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Interacts internally with team representatives from PCOR & Finance, Brands, Medical Affairs, HEOR, Commercial Pipeline, Field Sales, Account Management, Analytics, Investor Relations, Value Communication and Contracting Strategy colleagues across all franchises, and all others, including global colleagues/counterparts, on a routine basis.
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Safe and timely execution of Phase I studies; close collaboration with internal and external clinical study support staff and scientists (including discovery research, biostatistics, drug metabolism, modeling and simulation, regulatory affairs, and global clinical trials operations.
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The Medical Director for the SR Franchise is a key member of the Tissue Technologies Medical Affairs Leadership Team, reporting directly to the Head of Divisional Medical Affairs for the Tissue Technologies Division, and serving as a critical member of the Global Tissue Technologies and International teams to shape Integra Medical Affairs strategy and priorities.
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affairs job Title: sr associate in Lawrence, NJ
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