
1001 - 5000 funcionários
Fundada em 1995
💊 Farmacêutico
🏥 Saúde
Pharmaceuticals • Healthcare
A Eisai US é a filial nos Estados Unidos da Eisai Inc. , uma empresa farmacêutica global focada em pesquisar, desenvolver, fabricar e comercializar medicamentos — especialmente em neurologia (incluindo a doença de Alzheimer) e oncologia. Com quase 40 anos de presença em P&D e manufatura nos EUA, a Eisai US conduz ensaios clínicos, programas de apoio ao paciente, engajamento comunitário e iniciativas de responsabilidade corporativa sob sua missão de "assistência à saúde humana", e enfatiza um pipeline orientado pela ciência e colaborações para atender áreas de alta necessidade médica.
🕒 Julho 15
🏖️ New Jersey – Remoto
💵 $129.000 - $169.300 / ano
⏰ Tempo Integral
🟠 Sênior
👔 Gerente
👻 Score fantasma 2%
🗣️🇺🇸🇬🇧 Inglês obrigatório
Melhore suas chances de conseguir uma entrevista verificando sua pontuação de currículo antes de se candidatar.

1001 - 5000 funcionários
Fundada em 1995
💊 Farmacêutico
🏥 Saúde
Pharmaceuticals • Healthcare
A Eisai US é a filial nos Estados Unidos da Eisai Inc. , uma empresa farmacêutica global focada em pesquisar, desenvolver, fabricar e comercializar medicamentos — especialmente em neurologia (incluindo a doença de Alzheimer) e oncologia. Com quase 40 anos de presença em P&D e manufatura nos EUA, a Eisai US conduz ensaios clínicos, programas de apoio ao paciente, engajamento comunitário e iniciativas de responsabilidade corporativa sob sua missão de "assistência à saúde humana", e enfatiza um pipeline orientado pela ciência e colaborações para atender áreas de alta necessidade médica.
• Facilitate and lead the development, review, approval, and maintenance of the Company Core Data Sheets (CCDS) for assigned products • Represent the Global Regulatory Network (GRN) Global Labeling Group on project teams • Act as a Subject Matter Expert (SME) on local, regional and multi-country regulatory labeling requirements • Coordinate and lead cross-functional teams in the development and lifetime maintenance of the TPP, CCDS and Country Product Information (CPI) and CPI components for assigned products/projects • Provide tactical and strategic guidance to CPI development teams regarding regulatory requirements, content and design for TPP, CCDS, CPI and CPI components for assigned products on a global basis • Manage direct reports • Coordinate Content of Labeling/Drug Listing SPL generation and review to ensure compliance with US CPI regulations • Maintain labeling history documents and assist in responding to labeling-related queries.
• Minimum BS degree or higher in life science • 8+ years of experience in drug development environment, with minimum 3-5 years of regulatory experience within the pharmaceutical industry • Experience in global and/or local regulatory labeling environments is preferred • Demonstrate a solid working knowledge of drug development process, as well as FDA and EU labeling; knowledge of and experience with Asia and other markets labeling desirable • Competent knowledge of and demonstrated ability to apply regulatory guidelines pertaining to product labeling and ICH guidelines • Demonstrate strong project management, people management, problem solving, strategic thinking, negotiation, interpersonal and communication skills (both written and oral) attention to detail and ability to work under tight timelines.
• Eisai Inc. Annual Incentive Plan • Employees are eligible to participate in Company employee benefit programs.
Candidatar-se🕒 Julho 15
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