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 critical-thinking skills, with the ability to synthesize multiple evidence sources.
Ability to develop and communicate a clear rationale for feasibility assumptions and recommendations.
Strong attention to detail while maintaining awareness of the overall study strategy.
Ability to manage multiple concurrent deliverables, stakeholders, priorities, and deadlines.
Excellent written, verbal, and presentation skills.
Advanced proficiency in Microsoft Excel, PowerPoint, and Word.
Confidence working with web-based data, intelligence, and analytics platforms.
Strong ownership of deliverable quality, accuracy, and timeliness.
Collaborative working style and ability to operate effectively in a matrix environment.
Ability to work independently while seeking input and escalation appropriately.
Working knowledge of ICH-GCP principles.
Precision for Medicine brings together clinical-trial execution, scientific expertise, laboratory capabilities, and advanced data sciences to help life sciences organizations improve the speed, cost, and likelihood of successful clinical development. The organization has a strong focus on oncology and rare diseases and offers the opportunity to contribute to complex programs that seek to bring meaningful therapies to patients.
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Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law.
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Precision for Medicine is a clinical research organization (CRO) that provides comprehensive laboratory and bioservices solutions to support drug development and clinical trials. The company offers services spanning assay development, clinical testing, biorepository and sample management, logistics, and specialty lab services including biobanking and sample preparation. Precision for Medicine serves pharmaceutical, biotech, and clinical research clients globally, managing projects across multiple disciplines with a focus on accelerating the development and adoption of novel therapeutics. The organization operates with a client-facing approach, providing project management, contract management, and business development services to support the lifecycle of clinical studies and research initiatives.
