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The Legal, Corporate Administration, Regulatory Affairs, and Security (LCARS) Program Management Office (PMO) drives the successful execution of projects in State Street’s Legal, Regulatory Affairs, and Global Security divisions.
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Collaborate seamlessly with colleagues and departments, such as statistics and statistical programming, pharmacovigilance, clinical operations, regulatory affairs, medical directors, and other functions supporting clinical programs.
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Provide leadership for the MSL function by participating on cross functional teams leading to strategic planning and working collaboratively with Commercial colleagues including, Sales and Marketing as well as Medical Affairs.
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In partnership with the Director of Government Affairs, develop and implement engagement strategies for current and prospective MA elected officials, their staff, and coalition partners. Position Reporting to the Chief of Public Affairs, the Senior Political Manager will play an integral role within MCPSA’s Public Affairs department, and is responsible for leading execution of an advocacy and political agenda that will protect and create the conditions necessary for charter public schools in Massachusetts to thrive.
$83,500 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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About the OpportunityThe Office of External Affairs at Northeastern University is looking for a talented, hard-working, and highly motivated candidate to serve as the Executive Assistant to the Senior Vice President (SVP.
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As part of the Regulatory Affairs CMC team, you will report to the Executive Director and Head, CMC Regulatory Affairs – Pharmaceuticals. Join Takeda as a Senior Director, GRA CMC Pharmaceuticals Development Portfolio Lead where you will establish collaboration with Global CMC teams and leadership through networks and enable CMC regulatory team’s success in meeting goals/objectives.
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Core understanding of the medical device regulatory process in collaboration with Regulatory Affairs and provide essential support during internal and external audits and inspections by supplying necessary documentation and addressing findings related to design control and regulatory compliance.
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Work collaboratively with other Medical Directors, and colleagues in Biostatistics, Medical Writing, Drug Safety, Clinical Operations, Translational Medicine, and Regulatory Affairs. Collaborate with Regulatory Affairs to align studies with local, national and international health authority requirements.
$324,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Subject matter expertise in matters pertaining to behavioral threat assessment, both international and domestic (U.S.) affairs, and violent extremism as they pertain to the current threat environment.
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Our client, an advanced technology company, is seeking an Executive Assistant to partner with the SVP, Finance, and Government Affairs to manage their respective teams in a dynamic, rapidly changing, fast-faced environment.
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This role will report to the Senior Vice President, Global Value, Access, Public Policy and Government Affairs. This role is responsible for leading the HEOR development and execution of the global evidence teams, engaging closely with and guiding the product development teams across our pipeline, supporting our regions and affiliates, as well as leading our V&A engagement with external stakeholders on evidence and access.
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Master's Degree in College Student Personnel, Student Affairs, Psychology, or a related field required. Participate in conduct boards as assigned, adjudicate policy violations, update relevant software for each case, and serve as the primary hearing officer in your designated areas.
$48,950 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Build strong relationships with Student Affairs, Residence Life, Student Athlete Advisory Committee, Undergraduate Student Government, and the Campus Activity Board. Proven experience with the following applications and web development software: Adobe Premiere and PhotoShop, Adobe Illustrator, Microsoft Excel, Motion Graphics, Adobe InDesign, Javascript, HTML.
$79,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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CMC and GMP Knowledge: Deep understanding of CMC aspects of GMP development for both drug substance and drug product, with strong knowledge of quality, regulatory affairs, and manufacturing and supply.
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Assist in leading and supporting the medical affairs strategy for launching TTFields in NSCLC through a field based thoracic oncology MSL team. Attend and provide scientific support of US Medical Affairs activities and scientific sessions at relevant regional and national congress meetings and communicate insights internally.
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affairs job in Newtonville, MA
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