Feasibility Manager (Clinical Trials)

Location: Fully remote in the UK, Spain, Hungary, Poland, Romania, Serbia, or Slovakia

Company

Precision for Medicine combines clinical-trial execution, scientific expertise, laboratory capabilities, and advanced data sciences to support life sciences organizations with clinical development, particularly in oncology and rare diseases.

What you will do

• Lead or contribute to feasibility assessments for client requests for proposals across pre-award, post-award, rescue, and stand-alone engagements.
• Review clinical protocols, study assumptions, client information, and operational plans for United States and global clinical trials.
• Conduct and synthesize competitive landscape, historical recruitment, standard-of-care, treatment landscape, epidemiology, country, site, and patient-pool analyses.
• Translate evidence into country, site, enrollment, recruitment, and operational recommendations while identifying assumptions, data limitations, and feasibility risks.
• Present methods, findings, recommendations, and supporting rationale to internal stakeholders, proposal teams, and clients; participate in bid-defense meetings.
• Collaborate with cross-functional stakeholders, consultants, data partners, investigators, and sites, and contribute to feasibility tools, methods, templates, and best practices.

Requirements

• Bachelor’s degree in life sciences or a related discipline.
• At least two years of relevant experience in clinical-trial feasibility, clinical operations, site intelligence, epidemiology, clinical research, or a related area.
• Experience conducting or contributing to clinical-trial feasibility analysis and site or country identification.
• Ability to interpret clinical, scientific, epidemiological, and operational information and develop clear recommendations.
• Professional proficiency in written and spoken English.
• Advanced proficiency in Microsoft Excel, PowerPoint, and Word; confidence working with web-based data, intelligence, and analytics platforms; working knowledge of ICH-GCP principles.

Nice to have

• Postgraduate degree in life sciences, public health, epidemiology, data science, or a related discipline.
• Experience supporting global clinical trials or working in oncology, rare disease, or other complex clinical-development programs.
• Experience presenting analyses and recommendations to clients or senior stakeholders.
• Familiarity with clinical-trial intelligence, epidemiology, site-performance, claims, or real-world-data platforms.

Culture & Benefits

• Fully remote work within the listed European countries.
• Cross-functional collaboration across therapeutic areas and geographic regions.
• Opportunities to contribute to scientifically driven clinical-development programs.
• Knowledge sharing and professional development within the Feasibility team.