Global Study Manager – FSP EMEA

🔥 21 hours ago

🌐 United Kingdom, Poland, +4 more countries – Remote

🇬🇧 United Kingdom – Remote 🇵🇱 Poland – Remote 🇷🇴 Romania – Remote 🇮🇹 Italy – Remote 🇷🇸 Serbia – Remote 🇧🇪 Belgium – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

👔 Manager

👻 Ghost score 10%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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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

• Lead the operational strategy and end-to-end delivery of one or more global clinical studies • Own study timelines, budget, quality, risks and key operational deliverables • Provide strategic leadership to global, cross-functional study teams and drive timely decision-making • Represent Clinical Operations within the Study Leadership Team and act as the senior escalation point for operational issues • Translate clinical development and asset strategy into clear study-level operational plans • Lead proactive study risk identification, mitigation and issue resolution • Ensure robust feasibility, study planning and operational execution • Provide strategic operational input into protocols, informed consent forms and other key study documents • Oversee CROs and other external vendors, including vendor selection, performance management and escalation where deliverables are at risk • Ensure studies remain compliant with ICH-GCP, applicable regulations, SOPs and inspection-readiness requirements • Lead study financial planning, forecasting and budget management • Communicate study progress, risks, decisions and recommendations to senior stakeholders and governance forums • Champion innovative clinical trial delivery approaches, including decentralised trials, technology, automation and AI-enabled ways of working • Contribute to continuous improvement initiatives across Clinical Operations

🎯 Requirements

• Bachelor's degree in Life Sciences or a related discipline • Extensive experience in global clinical study delivery, ideally across multiple phases, indications and geographic regions • Proven experience holding end-to-end accountability for complex global clinical trials • Strong experience leading global cross-functional teams within a matrix environment • Demonstrated ownership of study timelines, budgets, risks, quality and operational strategy • Significant experience overseeing CROs and third-party vendors, including performance management and issue resolution • In-depth knowledge of ICH-GCP, global regulatory requirements and clinical development processes • Strong project and financial management capabilities • Ability to influence senior stakeholders and drive decisions in complex, fast-paced environments • Excellent leadership, communication, negotiation and conflict-management skills • Experience proactively identifying and resolving risks that could impact clinical programmes • Experience with Phase II and/or Phase III global clinical trials, adaptive or innovative trial designs, decentralised clinical trials, platform/umbrella/basket studies, technology-enabled delivery, automation or AI/ML, and working with investigators, external experts and regulatory authorities is highly desirable

🏖️ Benefits

• Fully remote work arrangement • Standard Monday-Friday work schedule