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The senior manager is responsible for the development of external integrated communication and public affairs (C&PA) strategies to support our Pulmonary Hypertension portfolio of products, primarily UPTRAVI, OPSUMIT, and OPSYNVI, as well as developing relevant content about diagnostics and treatment persistency to help bring awareness to this rare disease.
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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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Leading organizational and internal communications for scientific and regulatory affairs. Work closely with regulatory affairs and compliance teams to ensure that all communications adhere to industry regulations and guidelines.
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Serve as the USMA lead on solid tumor lifecycle strategy, including evidence generation strategy development and execution of Phase 3b/4 Medical Affairs led interventional and observational clinical trials; Ensures US market needs are satisfied within Integrated evidence generation plan; ensures development & updates of areas of interest reflective of US needs.
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As part of the GRA CMC Pharmaceuticals, Oligonucleotides team, you will report to the Executive Director and Head, CMC Regulatory Affairs, Pharmaceuticals. Join Takeda as a Director, GRA CMC Pharmaceuticals, Oligonucleotides where you will lead the GRA CMC Pharmaceuticals regulatory team in the development and implementation of global CMC regulatory strategies during development commercialization and post approval LCM stages.
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Proven track record of successful public relations/communications, corporate communications, product communications, public affairs, and/or media relations achievements. Lead the Communication & Public affairs strategies for the US Pulmonary Hypertension (PH) business, including UPTRAVI, OPSUMIT, and OPSYNVI in addition to leading launch readiness plans and communications for investigational therapies in Retina / Specialty Ophthalmology.
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The sections are: Community Affairs, State & Elections, Consumer Affairs Counseling, Education and Higher Education, Employment Counseling and Labor, Health and Human Services, and Law & Public Safety.
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Communicate frequently with other Respiratory Sales Specialists across the country and cross-functional counterparts such as Marketing, Sales Ops, Market Access, Field Reimbursement, Training, and Medical Affairs to create alignment of business plan, focus on strategic drivers, and sharing best practices.
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The incumbent will apply enterprise mindset and lead strategically across the BMS matrix by working with stakeholders from WW Medical and local market medical teams, Research & Early Development (R&ED), Global Drug Development (GDD), Health Economics & Outcomes Research (HEOR), Regulatory, Pharmacovigilance, Corporate Affairs, Competitive Intelligence, Legal, Business Insights & Analytics (BI&A) and other key functions.
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With funding for the next 2 years, they are now seeking an exceptional physician leader to serve as Chief Medical Officer and build out their full R&D function including clinical development, clinical operations, regulatory affairs, biometrics, medical affairs and drug safety.
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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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Certificate of Clinical Competence in Speech-Language Pathology (CCC-SLP) is required. The Speech-Language Pathologist (SLP) will access needs, plan strategies and deliver evidence based supports to students with communicative disabilities across a variety of educational settings to include general and special education classrooms, specialized schools and community settings.
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Qualifications: Education and Experience: Credentials: Master’s Degree in Speech-Language Pathology Pennsylvania Department of Education Certificate in Speech-Language Impaired PK-12 is required Certificate of Clinical Competence in Speech-Language Pathology (CCC-SLP) is required.
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10+ years of past relevant experience in the power and/or industrial sector as a project manager. Project teams in our Energy & Industrial Group (EIG) support industry-leading projects in power generation, plant design, environmental compliance, mid/downstream oil & gas, and multi-disciplined industrial projects.
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Qualifications: Education and Experience: Credentials: Master’s Degree in Speech-Language Pathology Pennsylvania Department of Education Certificate in Speech-Language Impaired PK-12 is required Certificate of Clinical Competence in Speech-Language Pathology (CCC-SLP) is required License to practice Speech Language Pathology issued by PA Bureau of Professional and Occupational Affairs is preferred.
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affairs job Title: regulatory affairs project manager in Trenton, NJ
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