Thermo Fisher Scientific
10,000+ employees
Founded 1956
🧬 Biotechnology
💊 Pharmaceuticals
🔬 Science
Biotechnology • Pharmaceuticals • Science
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.
FSP Feasibility Manager
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Thermo Fisher Scientific
10,000+ employees
Founded 1956
🧬 Biotechnology
💊 Pharmaceuticals
🔬 Science
Biotechnology • Pharmaceuticals • Science
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 strategic and operational feasibility activities for assigned clinical studies and development programs. • Drive evidence-based country selection by leveraging operational insights, historical performance, epidemiology, and data analytics to support optimal study execution. • Develop and deliver data-driven recruitment strategies and enrollment forecasts in collaboration with Feasibility Analysts and cross-functional study teams. • Evaluate country, site, and patient recruitment potential using internal and external data sources and feasibility tools. • Partner with sponsor and Thermo Fisher Scientific stakeholders to develop robust feasibility strategies that support study planning and delivery. • Build and maintain strong collaborative relationships with Clinical Operations, Clinical Sciences, Medical Affairs, Regulatory Affairs, Clinical Supply, Country Operations, Site Activation, Epidemiology, Biostatistics, and other key functional partners. • Present feasibility recommendations and enrollment assumptions to study teams and governance groups, providing clear rationale and risk assessments. • Identify recruitment risks and propose proactive mitigation strategies throughout study planning and execution. • Support portfolio-level planning by providing feasibility intelligence across multiple studies and therapeutic areas where required. • Lead or contribute to cross-functional feasibility working groups and study planning meetings. • Serve as a subject matter expert (SME) for feasibility methodologies, systems, and analytical tools. • Support the evaluation, implementation, and continuous improvement of feasibility processes, technologies, and data analytics solutions. • Ensure all feasibility activities are conducted in compliance with sponsor requirements, SOPs, ICH-GCP, regulatory guidelines, and Thermo Fisher Scientific quality standards. • Contribute to process improvement initiatives that enhance the quality, efficiency, and consistency of feasibility deliverables across the FSP organization.
🎯 Requirements
• Bachelor's degree in Life Sciences, Pharmacy, Nursing, Public Health, or a related scientific discipline. • 4–7 years of experience in study feasibility • Experience supporting global or regional clinical trial feasibility activities. • Demonstrated understanding of global clinical trial planning, country selection, site identification, and patient recruitment strategies. • Strong understanding of the drug development process and global clinical research regulations, including ICH-GCP and applicable regulatory guidelines. • Knowledge of country and site feasibility methodologies, enrollment forecasting, and recruitment planning. • Experience using clinical trial intelligence and recruitment platforms such as Citeline, TriNetX, DQS, GlobalData, or similar tools. • Strong analytical skills with experience interpreting complex datasets and translating findings into actionable recommendations. • Proficiency in data visualization and reporting tools, including Microsoft Excel and PowerPoint; experience with Power BI or similar platforms is advantageous. • Excellent verbal, written, and presentation skills with the ability to communicate effectively across technical and non-technical audiences. • Strong stakeholder management and influencing skills, with the ability to build collaborative relationships across sponsor and Thermo Fisher Scientific teams. • Excellent organizational, planning, and prioritization skills with the ability to manage multiple studies simultaneously. • Demonstrated problem-solving abilities and sound decision-making skills. • High attention to detail with a commitment to quality and continuous improvement. • Ability to work independently while contributing effectively within global, matrixed teams.
🏖️ Benefits
• Flexibility to support global teams across multiple time zones • Occasional travel may be required for business meetings, client engagements, or team events
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