Project Manager, Internal Medicine – Metabolic Live Diseases

🕒 Agosto 19

🌐 Estados Unidos, Canadá – Remoto

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🌲 North Carolina – Remoto

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💵 $112.000 - $222.000 / ano

⏰ Tempo Integral

🟡 Pleno

🟠 Sênior

👷‍♀️ Gerente de Projetos

🦅 Patrocina Visto H1B

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👻 Score fantasma 0%

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🗣️🇺🇸🇬🇧 Inglês obrigatório

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Logo of Worldwide Clinical Trials

Worldwide Clinical Trials

1001 - 5000 funcionários

🏥 Saúde

💼 Consultoria

📦 Logística

Healthcare • Consulting • Logistics

Worldwide Clinical Trials é uma organização global de pesquisa clínica por contrato (CRO) que oferece serviços abrangentes de ensaios clínicos. A empresa é especializada em apoiar estudos em diversas áreas terapêuticas, como oncologia, cardiologia e doenças raras. Com mais de 30 anos de experiência, a Worldwide Clinical Trials enfatiza suporte personalizado e soluções sob medida ao longo de todo o ciclo de vida do desenvolvimento de medicamentos. Seus serviços incluem monitoramento clínico, gestão de dados, recrutamento de pacientes e consultoria regulatória, garantindo precisão e atenção personalizada para cada ensaio clínico.

Descrição

• Manage one or more allocated Phase I through IV clinical trials, which may be local, regional, or global • Coordinate and manage clinical trials from start-up through close-out activities • Direct the technical, financial, and operational aspects of projects • Work with functional area leads to identify and evaluate project requirements • Interpret data on complex issues • Plan for contingencies and implement rescue strategies when needed • Ensure solutions are implemented and project deliverables meet customer time, quality, and cost expectations • Lead core project team members and facilitate leadership of extended or complete project teams • Lead internal and external cross-unit coordination, including subcontractors • Define and manage project resource needs with functional heads • Establish contingency plans for key resources • Ensure successful design, implementation, tracking, and revision of project plans • Promote effective teamwork and resolve conflicts • Communicate project-related matters to Project Management management

🎯 Requisitos

• University/college degree (life science preferred) or certification in a related allied health profession from an appropriately accredited institution, or equivalent combination of education and experience • Minimum of five (5) years of clinical pharmaceutical industry experience, including clinical project management tasks • Alternatively, more than five (5) years supervisory experience in a health care setting and four (4) years clinical research experience in the pharmaceutical or CRO industries, or proven relevant clinical development experience and skills • Thorough knowledge of project management processes • Thorough knowledge of ICH Guidelines and GCP, including international regulatory requirements • Available for domestic and international travel, including overnight stays • Valid current passport required • Ability to drive and have a valid driver’s license • Fluent in local office language and English, written and verbal • Broad knowledge of drug development processes and client needs • Experience managing projects in a multi-office environment • Ability to handle multiple competing priorities and utilize resources effectively • Ability to inspire teamwork and motivate staff within a matrix system • Ability to lead by example and encourage team members to seek solutions • Excellent communication, planning, and organizational skills

🏖️ Benefícios

• Competitive benefits package depending on location • Transparent compensation and pay equity

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