Feasibility Manager
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Job Description
Feasibility Manager assessing clinical-trial feasibility for Precision for Medicine. Analyzing recruitment, site, country, epidemiology, and patient-pool data for life sciences clients.
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.
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.
- Equivalent combinations of education, qualifications, and relevant experience may be considered.
- Experience supporting global clinical trials preferred.
- Experience in oncology, rare disease, or other complex clinical-development programs preferred.
- Experience presenting analyses and recommendations to clients or senior stakeholders preferred.
- Familiarity with clinical-trial intelligence, epidemiology, site-performance, or claims and real-world-data platforms preferred.
- 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.
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