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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.
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Serve as a CMC strategist and project leader for projects/programs, providing regulatory assessments and developing regulatory strategies with input from the Executive Director Regulatory Affairs CMC.
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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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Work may focus on issues including technology and geopolitics, the energy transition, the Middle East, transatlantic relations, U.S.-China relations, and other topics in U.S. foreign policy and international affairs.
$85,043 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Candidates with experience in the following roles are preferred: Policy Analyst, Policy Associate, Communications Analyst, Communications Associate, Regulatory Affairs Analyst, Regulatory Affairs Associate, Regulatory Analyst, Regulatory Associate.
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Affairs CMC Submissions. Management in Lexington, MA to establish global submission activities and timelines in partnership with global and cross-functional stakeholders in Pharmaceutical Science, GMS, Biologics.
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The candidate will work directly with pharmaceutical partners, R&D scientists, Clinical Trial Managers/ Clinical Research Associates, Quality Assurance, and Regulatory Affairs to assure compliance with internal and external requirements.
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Work in partnership with project managers in Supply Chain, Manufacturing, Finance, Human Resources, Marketing, Commercial, Medical Affairs and Market Access to ensure that contract negotiations advance in alignment with operational objectives.
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The MSL is a key member of the medical affairs team, collaborating with cross-functional teams and building strong relationships with KOLs and other stakeholders to support the best possible patient outcomes.
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Typically requires 10 years of relevant pharmaceutical or biotech industry experience within regulatory affairs, or the equivalent combination of education and experience. Advanced technical skill in regulatory affairs science including knowledge of regulatory frameworks and external environments.
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You enjoy working closely with the project teams, particularly Clinical Operations, Regulatory Affairs, and clinical and nonclinical development teams, to manage all aspects of clinical/regulatory document preparation, including protocols, CSRs, Investigator Brochures, and other regulatory submission documents.
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Citigroup Inc. and its subsidiaries ("Citi”) invite all qualified interested applicants to apply for career opportunities. Citi offers competitive employee benefits, including: medical, dental & vision coverage; 401(k); life, accident, and disability insurance; and wellness programs.
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Seven Letter specializes in strategic public affairs communications, brand and reputation management, digital community building and engagement, and crisis communications for corporate, nonprofit and industry advocacy clients.
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10 years of relevant professional experience, including at least 3 years in Regulatory Affairs in a U.S. advertising and promotion role. Collaborate with colleagues in Commercial, Medical Affairs, Legal, Compliance and other expertise areas in creation of promotional and disease awareness communications, field training materials, and materials and communications used in scientific exchange, for assigned product(s.
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Stakeholder Collaboration: Collaborate with Indication Development Teams and cross-functional partners, including Trial Operations, medical affairs, regulatory affairs, global patient advocacy, and Global Sourcing & Vendor Alliance Management (GloSAM.
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affairs job Company: Citi in Cambridge, MA
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