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Precision for Medicine is seeking a Senior Feasibility Manager to join its European Feasibility Department. This fully remote role is available across the UK, Spain, Hungary, Poland, Romania, Serbia, and Slovakia. The position combines clinical and scientific interpretation with operational intelligence and data analysis to deliver evidence-based feasibility assessments for clinical trials.
You will be responsible for leading or contributing to feasibility assessments across pre-award, post-award, rescue, and stand-alone engagements. Key responsibilities include reviewing clinical protocols and study assumptions, conducting competitive landscape and recruitment analyses, synthesizing epidemiological and operational data, and translating evidence into clear country, site, enrollment, and operational recommendations. You will present findings to internal stakeholders and clients, collaborate with cross-functional teams including Business Development and Clinical Operations, and participate in bid-defense meetings.
The role requires strong analytical skills to interpret clinical, scientific, epidemiological, and operational information. You will manage multiple concurrent deliverables, develop transparent rationales for assumptions, identify data limitations and feasibility risks, and contribute to the development of feasibility methods and best practices within the team.
Required qualifications include a bachelor's degree in life sciences or related discipline, at least two years of relevant experience in clinical trial feasibility, clinical operations, site intelligence, epidemiology, or clinical research, and demonstrated ability to conduct feasibility analysis and site/country identification. Professional proficiency in written and spoken English is essential.
Preferred qualifications include a postgraduate degree in life sciences, public health, epidemiology, or data science; experience supporting global clinical trials; expertise in oncology or rare disease programs; experience presenting to clients or senior stakeholders; and familiarity with clinical-trial intelligence platforms or real-world data sources. Advanced proficiency in Excel, PowerPoint, and Word, along with working knowledge of ICH-GCP principles, is valued.
