SlipstreamJobs tracks this role from the company's public career site. Apply directly on the employer's site.
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 final title (Senior Feasibility Associate or Feasibility Manager) will be determined based on the candidate's experience and demonstrated responsibility level.
The Feasibility Manager delivers evidence-based feasibility assessments for clinical trial engagements across pre-award, post-award, rescue, and stand-alone projects. 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, study assumptions, 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; presenting findings to internal and external stakeholders; collaborating with colleagues, consultants, data partners, and investigators; coordinating site and investigator outreach; participating in bid-defence 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, 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; oncology or rare disease experience; client presentation experience; familiarity with clinical-trial intelligence or real-world-data platforms.
Essential skills: strong analytical and critical-thinking abilities; clear communication of feasibility rationale; attention to detail; ability to manage multiple concurrent deliverables and stakeholders; excellent written, verbal, and presentation skills; advanced Microsoft Office proficiency; confidence with web-based data and analytics platforms; ICH-GCP working knowledge; collaborative matrix-environment experience.
