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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 to candidates in the UK, Spain, Hungary, Poland, Romania, Serbia, or Slovakia.
The Feasibility Manager delivers evidence-based feasibility assessments for clinical trials across pre-award, post-award, rescue, and standalone engagements. The role combines clinical and scientific interpretation with operational intelligence and data analysis to develop country, site, patient-pool, and recruitment recommendations. You will partner with Business Development, Clinical Operations, Medical, and cross-functional stakeholders to ensure recommendations are scientifically credible, operationally realistic, and clearly communicated.
Key responsibilities include leading or contributing to feasibility assessments for client RFPs; reviewing clinical protocols and operational plans for US and global trials; conducting competitive landscape, recruitment, epidemiology, and patient-pool analyses; translating evidence into clear recommendations; developing transparent rationales for assumptions and identifying feasibility risks; presenting findings to internal stakeholders and clients; collaborating with internal colleagues, external consultants, data partners, investigators, and sites; planning and analyzing targeted outreach; participating in bid-defense meetings; and contributing to the development of feasibility methods, tools, and best practices.
Required qualifications: 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; experience conducting or contributing to feasibility analysis and site/country identification; ability to interpret clinical, scientific, epidemiological, and operational information; professional English proficiency.
Preferred qualifications include postgraduate degree in life sciences, public health, epidemiology, or data science; experience supporting global clinical trials; experience in oncology or rare disease programs; experience presenting to clients or senior stakeholders; familiarity with clinical-trial intelligence platforms or real-world data sources.
Essential skills: strong analytical and critical-thinking abilities; ability to synthesize multiple evidence sources; clear communication of feasibility rationales; attention to detail; ability to manage multiple concurrent deliverables and stakeholders; excellent written, verbal, and presentation skills; advanced proficiency in Excel, PowerPoint, and Word; confidence with web-based data and analytics platforms; strong ownership of quality and timeliness; collaborative working style; ability to work independently; working knowledge of ICH-GCP principles.
