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As a deputy to the executive director of Public Affairs, the Director will ensure the integration of UCSF Health's marcomm strategies with the Public Affairs team's media relations and owned content strategies supporting UCSF's clinical, research, education, public service missions.
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AA&PI Student Services is part of the Division of Equity & Community Inclusion under Student Affairs & Enrollment Management. Work in collaboration and partnership with other programs, departments, and areas within Student Affairs & Enrollment Management and in Academic Affairs to support Pacific Islander student needs for program planning, course advisement, major and career exploration.
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The Department is organized into four divisions: Housing, Community Development, Homeownership and Below Market Rate Programs, and Finance and Administration, and includes additional teams that report directly to MOHCD’s Director including: Communications, Policy and Legislative Affairs, and Place-Based Initiatives.
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Oversee execution of workstreams by directing and coordinating resources in the transmission, government affairs, permitting and development teams. Or add your expertise to our supply and trading operations, brokering renewable electricity, green gas, commodities, and CO2 emission allowances from one of our advanced energy trading floors.
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Experience in advertising and promotional regulatory affairs activities through launch and commercialization are a plus. The VP, Regulatory Affairs will provide strategic regulatory expertise to support the continued development and the commercialization of acoramidis for the proposed treatment of ATTR-CM and the prevention of ATTR. This role involves collaboration with cross-functional project teams in planning and execution of development strategies while providing leadership to global regulatory submissions.
$305,000 - $365,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Identify laboratories to publish abstracts working with Scientific Affairs in support of Hologic Diagnostic products and product launches. Minimum of 3 years related experience as Cytotechnologist, or 1-year experience with a master’s degree in gyn and non gyn cytology as Cytotechnologist.
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Lead the medical affairs strategy congress activity planning in collaboration with team members and compiling of congress reports including critical competitive intelligence. You will manage the global medical affairs strategic plans, including publication strategy, communication strategy, disease awareness, and asset strategy across Vir's HBV functional cure pipeline.
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POSITION SUMMARY Reporting to the Managing Counsel, Health Affairs, Privacy & Data Protection Law, the Principal Counsel - Health Regulatory provides primary legal support to the University's medical centers and health sciences schools on complex and high impact healthcare regulatory analysis.
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Serve as principal Compliance reviewer for the Corporate Affairs Grants Review Committee (GRC). JD degree with a minimum of 5-10 years of experience as in-house counsel or associate at a major law firm with a background in biotechnology, pharma or healthcare related matters.
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OPPORTUNITY Mammoth is hiring a Director/Sr. Director, Regulatory Affairs, Therapeutics, to lead the regulatory activities of our growing CRISPR-based therapeutic programs as we bring them from concept to market.
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Work cross-functionally with the Regulatory Affairs, Scientific Affairs, Brand Strategy and Project Management Teams to ensure on-pack and supporting product copy is clear, concise and delightfully disruptive.
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12+ years of legal experience as an attorney, including experience at an established law firm and in-house at entertainment/media companies, with 8+ years of extensive experience negotiating and drafting a wide range of entertainment-related agreements and 3+ years of legal experience in a business and legal affairs role focusing on original scripted series content production.
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Be a strategic partner to Pliant's Research, Clinical, Pipeline Marketing, Legal, Business Development, Regulatory Affairs and Human Resources teams as well as employee-centric including Employee Experience and Diversity, Equity, and inclusion (DEI.
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Experience with R&D, Brand, Quality Assurance / Quality Control, Regulatory Affairs, Clinical, Manufacturing environments regulated by the FDA. This position is responsible for the business analysis, planning, project management, implementation, computer systems validation and ongoing support of business applications in the areas of Research & Development Analytical, Regulatory Affairs, Clinical, Quality Affairs and Quality Control.
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It is highly desirable that the candidate possess strong written and communications skills to collaborate successfully with the SFMTA Board, MTA Executive Team, Transit Division Senior Management, Operations and Maintenance Team, Technology Solution and Integration Team, MTA Legal Team, Government Affairs, Communications Team, Peer Transit Agencies, and Federal and State Agencies.
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affairs job Company: Medxcel in San Francisco, CA
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