Global Senior Project Manager – FSP

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Thermo Fisher Scientific

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1956

🏥 Healthcare

📦 Logistics

🏭 Manufacturing

Healthcare • Logistics • Manufacturing

Thermo Fisher Scientific is the world leader in serving science, with annual revenue of more than $40 billion. Their mission is to enable customers to make the world healthier, cleaner, and safer by supporting life sciences research, solving complex analytical challenges, increasing laboratory productivity, and improving patient health through diagnostics and the development of life-changing therapies. With a global team, they offer innovative technologies and pharmaceutical services through brands such as Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD.

📋 Description

• 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

🎯 Requirements

• 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)

🏖️ Benefits

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