Feasibility Manager – Clinical Trial Feasibility

About the role

Precision for Medicine is expanding its European Feasibility Department and seeks a Feasibility Manager (or Senior Feasibility Associate) to work remotely across several European countries. The role blends clinical and scientific interpretation with operational intelligence to deliver evidence‑based feasibility assessments for clinical trials.

Key responsibilities

• Lead or contribute to feasibility assessments for client RFPs, covering pre‑award, post‑award, rescue and stand‑alone projects.
• Review clinical protocols, study assumptions and operational plans for US and global trials.
• Conduct competitive‑landscape, historical recruitment, standard‑of‑care, treatment‑landscape, epidemiology, country, site and patient‑pool analyses.
• Translate evidence into clear country, site, enrolment and operational recommendations.
• Develop transparent rationales for assumptions, identify data limitations and feasibility risks.
• Present methods, findings and recommendations to Business Development, proposal teams and clients.
• Collaborate with internal colleagues, external consultants, data partners, investigators and sites to gather feasibility information.
• Plan, coordinate and analyse targeted site and investigator outreach as needed.
• Participate in bid‑defence meetings and client discussions.
• Contribute to the evolution of feasibility methods, data sources, tools, templates and best practices, and mentor junior team members.

Required profile

• Bachelor’s degree in life sciences or a related discipline.
• Minimum two years of experience in clinical trial feasibility, clinical operations or a related field.
• Strong analytical mindset with the ability to synthesize complex data into actionable recommendations.
• Excellent communication skills for presenting findings to internal and external stakeholders.

Required skills

What we offer

• Fully remote work arrangement across the UK, Spain, Hungary, Poland, Romania, Serbia or Slovakia.
• Opportunity to shape feasibility strategy within a fast‑growing, science‑driven organization.
• Collaborative, cross‑functional environment with exposure to global clinical trial programs.