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As lead of the Study Core Team the CS will lead via a matrix organization Epidemiology, Biostats, Clinical Operations, Medical/Scientific Affairs, Regional, Pfizer laboratory assay group, and external team members.
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Is offering a two-year Health Economics and Outcomes Research (HEOR) / Medical Affairs PharmD fellowship based in Newton, MA. Medical Affairs assignments will be tailored to align with the candidate's interests in areas such as Scientific Communications, Field Responsibilities, Advisory Boards, and Symposiums.
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This position will also play an important role communicating with the Red Sox’ local neighbors, planning and attending meetings and events at Fenway Park and in the area, working on strategic initiatives, and assisting with a wide array of administrative matters relating to Government & Neighborhood Affairs and also for the Legal Department.
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A or B.S. degree, MS preferred, in an appropriate scientific field with 15+ years’ experience in Pharmaceutical/Biotech Industry with 10+ years in a CMC Regulatory Affairs capacity. The Senior Director, CMC Regulatory Affairs reports to the VP, Regulatory Affairs and develops and executes CMC regulatory strategies and activities.
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Supervise and support reporting units, including Communications, Legislative Affairs, Constituent Services, Hiring and Staffing (Human Resources Liaison office), Federal Policy, Member Engagement, Housing and Homelessness Policy, and MassHealth’s Project Management Office.
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7+ years of government affairs experience working public policy issues related to consumer protection and data privacy. Government Affairs (GA) is responsible for advocating Motorola Solutions' public policy positions with policymakers in the United States and abroad.
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This position is hybrid, based in Santa Monica, CA, and reports to the Executive Director, CMC Regulatory Affairs. The AD CMC Regulatory Affairs supports the development and successful performance of the CMC regulatory strategy for the innovative pipeline of early-stage T cell therapies.
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This role will partner closely with key functions across Takeda Oncology including Translational Medicine, Clinical, Sciences, Global Regulatory Affairs, the Oncology Business Unit (Commercial and Medical Affairs), Alliance Management, Business Development, and clinical biomarker technologies.
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Participate in CMC project team meetings and provide Regulatory CMC support as needed, including update to the teams on follow-up actions, information request, risk assessment and mitigation in support of clinical trial application and marketing application.
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MedPro is one of the largest recruiters of therapists and nurses from outside the U.S. MedPro currently has contracts with numerous organizations to service a multitude of facilities in the U.S. The company counts among its clients prominent healthcare facilities and organizations such as the Department of Veterans Affairs,HCA, University of Miami Hospital, and Tenet Healthcare.
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Build and lead effective partnerships with internal stakeholders, including Medical Affairs directors, Clinical Development, Biostatistics, Legal, Discovery, Field Medical, HEOR and cross-functional members of publication teams.
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These offices include the Admissions, Financial Aid, Academic Affairs, Advanced Graduate Education, International Affairs and the Health Science Bursar's Office. Direct registrar, academic affairs, or student affairs experience in graduate or professional school setting is preferred and will be considered in lieu of experience in other student services areas.
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Accomplished policy advocacy professional with at least 15 years of experience in public affairs (government affairs and/or policy). Lead development and implementation of global policy advocacy strategy on key global policy topics including engagement with multilateral institutions, international trade association engagement, and LOCs in close collaboration with Takeda’s Enterprise Public Affairs Leadership Team (EPALT.
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The CCMO partners with Harvard Public Affairs and Communications and the HDS associate dean for development and external relations regarding media events, external relations, and campaign communications strategy and implementation.
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The Regulatory Affairs Specialist (RAS) positions are critical to successfully achieving ongoing clinical research expansion and regulatory compliance at DFCI. The Regulatory Affairs Specialist (RAS) positions provides advanced expertise and regulatory support to 600+ investigators and research staff members at DFCI, focusing on standards and techniques for performing job functions typical in the development and/or conduct of FDA regulated research from an operational and regulatory compliance perspective.
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affairs job Title: assistant Company: Citi in Boston, MA
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