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Regularly interfaces with team members in R&D including Biostatistics and SAS Programming staff, Data Management, clinical research and operations teams, regulatory affairs, clinical pharmacology, medical writing, medical affairs and quality management.
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Support project teams, regulatory affairs, product management, marketing, and product stewardship in topics related to toxicology and kinetics. The position is located in Princeton, NJ and is part of the global Regulatory Affairs Toxicology Group.
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Assist the Clinical Program Director, Program Supervisor and Lead Housing Specialist in communicating with the Department of Community Affairs and HUD with Project Managers for COC vouchers for chronically homeless individuals in Mercer County.
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Lead through Internal Collaboration : Forge strong collaborations with clinical development, medical affairs, market access, and regulatory teams to ensure seamless integration of Access strategies into overall product development and market access plans Lead in External Agency Management : Provide hands-on oversight and guidance on HEOR and pricing related agency selection and management, ensuring the highest quality of collaborations at proper cost.
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Associate Director, Global Regulatory Affairs Operations, Authoring Support page is loaded. Associate Director, Global Regulatory Affairs Operations, Authoring Support.
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This position will be responsible for supporting and contributing to the development and execution of robust health economics, outcomes research, epidemiology and real-world evidence plans that are aligned with brand strategies, medical affairs strategies, clinical development plans, support product value propositions, and optimize market access.
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The Product Director must work closely with multiple functions including Sales, Sales Learning & Development, Commercial Insights & Strategy, Medical Affairs, Global Strategic Marketing, Communications, Regulatory, Health Care Compliance (HCC), Innovative Medicine affiliates, outside vendors and Key Opinion Leader speakers to effectively implement key commercial activities.
$118,000 - $177,000 a yearFull-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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BDI is based at the Princeton School of Public and International Affairs (SPIA), co-hosted by the Empirical Studies of Conflict. Build BDI’s state-based partnerships and relationships with key stakeholders representing varying sectors including election protection, racial justice, LGBTQ+ rights, faith-based, government, and others in order to provide monitoring and analysis support across the board and to better inform our research.
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Interacts internally with team representatives from 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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The base salary range for the Director, Real World Evidence, Global Medical Affairs is from :213,500-280,200 Under current guidelines, this position is eligible to participate in : Eisai Inc. Annual Incentive Plan & Eisai Inc. Long Term Incentive Plan.
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Summary of JobThe Scientific Director, reporting into the Global MA Product Head Mogamulizumab, will support the Global MA Product Head in the planning and execution of Global Medical Affairs activities for mogamulizumab in hematology-oncology, building and facilitating highly effective collaborations and alignment with regional and country medical leadership, as well as other key cross-functional stakeholders.
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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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They will partner with US and WW Commercial, Research and Development, HEOR and Regulatory Affairs to support NULOJIX, SPYRCEL, ABRAXANE and other Established Brands. + Experience in working as a project member of a multi -functional team, knowledge of the US Medical Affairs organization, medical planning and regulatory landscape are desirable.
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Partner with Marketing, Public Relations/Communications, and Government Affairs to develop content and materials regarding corporate social responsibility mission and progress. Must be conversant in corporate responsibility, social issues, DEI, and best practices, including philanthropy, environmental sustainability, community affairs, and volunteerism.
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License to practice Speech Language Pathology issued by PA Bureau of Professional and Occupational Affairs is preferred. Will consider strong Clinical Fellowship Year (CFY) candidate for Long Term Substitute (LTS) positions in the Related Services program.
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affairs job Title: regulatory affairs associate Company: Thermo Fisher Scientific in Lawrence, NJ
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