Senior Project Manager – FSP

🔥 1 minute ago

🇧🇪 Belgium – Remote

⏰ Full Time

🟠 Senior

👷‍♀️ Project Manager

👻 Ghost score 10%

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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

• Serve as the client-embedded Project Lead and primary sponsor contact • Own overall project delivery across quality, time, and cost • Establish and communicate customer expectations to the project team • Lead cross-functional project teams and manage increasingly complex projects • Coordinate study teams, stakeholders, and CRO/vendors • Deliver clinical studies end-to-end while aligning with sponsor processes, tools, and performance measures • Oversee study timelines, budgets, CRO/vendor deliverables, out-of-scope activities, and contract modifications • Lead risk management, mitigation, issue escalation, and resolution • Lead a complex rescue/transition study, including transition planning, financial oversight, reconciliation, risk identification, and cross-functional coordination • Provide ICF Project Management within Medical Writing, overseeing global informed consent form development and protocol amendment implementation • Manage sponsor review, country customization, translation readiness, and accelerated delivery timelines • Maintain communication across study teams, sponsors, and stakeholders in compliance with regulatory requirements and ICH-GCP standards

🎯 Requirements

• Bachelor's degree or equivalent and relevant formal academic / vocational qualification • 8+ years of previous relevant experience • Biotech experience is a plus • Rare disease, auto-immune, and/or oncology clinical trial background is a plus • Technical and systems competency, including Microsoft Outlook, Word, Excel, PowerPoint, MS Project, CTMS, TMF, IWRS, eCOA, and eCRF databases • Ability to delegate and prioritize workload and resources in a changing environment • Effective oral and written communication and presentation skills • In-depth therapeutic area knowledge and clinical development guidelines and directives • Advanced knowledge of cross-functional project management principles across time, quality, and cost • Ability to lead, motivate, and coordinate cross-functional project teams • Strong customer service, negotiation, financial acumen, judgment, critical thinking, and strategic thinking skills • Ability to work independently with minimal supervision

🏖️ Benefits

• Collaboration and development opportunities • Environment supporting passion, innovation, and scientific excellence

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