Feasibility Manager

Before you apply

Job source

Himalayas

Applying on

himalayas.app

Workplace

Fully remote

US state

Nationwide remote

Category

Virtual Assistant

Link last checked

Not checked yet

Posted

2 weeks ago

Closes

11/2/2026

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About the role

Due to our continued growth, Precision for Medicine is looking for a Senior Feasibility Associate/Feasibility Manager to join our European team. This position can be covered fully remotely in UK, Spain, Hungary, Poland, Romania, Serbia or Slovakia. The final title, Senior Feasibility Associate or Feasibility Manager, will be determined based on the successful candidate’s experience and demonstrated level of responsibility. Position Summary: The Feasibility Manager is a member of Precision for Medicine ’s expert Feasibility Department and is responsible for delivering evidence-based feasibility assessments across pre-award, post-award, rescue, and stand-alone engagements. The role combines clinical and scientific interpretation with operational intelligence and data analysis to develop country, site, patient-pool, and recruitment recommendations. The Feasibility Manager partners with Business Development, Clinical Operations, Medical, and other cross-functional stakeholders to ensure that recommendations are scientifically credible, operationally realistic, and clearly communicated. The successful candidate will manage assigned feasibility deliverables, present analyses and recommendations to internal stakeholders and clients, and contribute to strategic initiatives that strengthen Precision for Medicine ’s feasibility capabilities and competitive position. Key responsibilities Lead or contribute to feasibility assessments for client requests for proposals. Review clinical protocols, study assumptions, client information, and operational plans for United States and global clinical trials. Conduct and synthesise 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 logical, transparent rationales for assumptions and identify important data limitations and feasibility risks. Present feasibility methods, findings, recommendations, and supporting rationale to Business Development colleagues, proposal teams, and clients. Collaborate with internal colleagues, external consultants, data partners, investigators, and sites to gather and interpret feasibility information. Plan, coordinate, and analyse targeted site and investigator outreach, as appropriate. Participate in bid-defence meetings and client discussions. Contribute to the continued development of feasibility methods, data sources, tools, templates, and best practices. Share knowledge and support the development of colleagues within the Feasibility team. Work effectively across functions, therapeutic areas, and geographic regions. Contribute to initiatives that strengthen Precision for Medicine ’s scientifically driven approach and client offering. Required qualifications and experience: 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. Equivalent combinations of education, qualifications, and relevant experience may be considered. Preferred qualifications and experience Postgraduate degree in life sciences, public health, epidemiology, data science, or a related discipline. Experience supporting global clinical trials. Experience 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, or claims and real-world-data platforms. Skills Strong analytical and cri

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