Global Senior Project Manager – FSP

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🕒 Julho 25

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Thermo Fisher Scientific

SiteLinkedInTodas as Vagas

10.000+ funcionários

Fundada em 1956

🏥 Saúde

📦 Logística

🏭 Manufatura

Healthcare • Logistics • Manufacturing

A Thermo Fisher Scientific é a líder mundial em servir à ciência, com receita anual de mais de US$ 40 bilhões. Sua missão é capacitar os clientes a tornar o mundo mais saudável, limpo e seguro, apoiando a pesquisa em ciências da vida, solucionando desafios analíticos complexos, aumentando a produtividade dos laboratórios e melhorando a saúde dos pacientes por meio de diagnósticos e do desenvolvimento de terapias que transformam vidas. Com uma equipe global, oferece tecnologias inovadoras e serviços farmacêuticos por meio de marcas como Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon e PPD.

Descrição

• Own the day-to-day management of the global clinical study • Lead cross-functional study teams (clinical operations, data management, biostatistics, medical monitoring, regulatory, supply chain, safety, etc.) • Ensure alignment between global strategy and regional execution • Drive study timelines, milestones, and deliverables • Develop and maintain study timelines, operational plans, risk management plans, enrollment strategies • Oversee country start-up, site activation, recruitment, monitoring, and closeout • Manage external vendors and CRO partners • Monitor study budgets and forecasts • Identify study risks early • Ensure study conduct follows ICH-GCP local regulations SOPs protocol requirements • Communicate updates to senior leadership, study teams, regional teams, sponsors/partners • Monitor enrollment, data cleaning, query resolution, and database lock readiness • Make operational decisions that impact study delivery

🎯 Requisitos

• Bachelor’s degree: life sciences or related discipline • At least 6+ years of relevant study management experience on a global level • In-depth experience in clinical research: study management, monitoring, data management • Previous in-depth Oncology experience • Must have exposed to clinical study management “end-to-end” • Must have proven experience from study feasibility to CSR • Must have at least Ph II and PIII experience • Must have cross-functional leadership proven experience • Able to input in clinical protocol, ICF, and other study plan • Strong experience in clinical budget management • Strong experience with vendor management including CRO • Exposed to competent authority Inspections (FDA, EMA, MHRA, PMDA) • Fluent in English, to the level they can negotiate and discuss related to complex topics with any Clinical team member • Excellent stakeholder management and communication skills (oral and written)

🏖️ Benefícios

• Health insurance • 401(k) matching • Flexible working hours • Paid time off • Remote work options