Feasibility Manager
P
Precision for MedicineClinical trials
This position can be covered fully remotely in UK, Spain, Hungary, Poland, Romania, Serbia or Slovakia.Full-TimeManager
Salary not disclosed
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Job Details
- Languages
- Professional proficiency in written and spoken English.
- Experience
- At least two years of relevant experience in clinical trial feasibility, clinical operations, site intelligence, epidemiology, clinical research, or a related area.
- Required Skills
- Microsoft ExcelPowerPoint
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.
- Strong analytical and critical-thinking skills, including synthesizing multiple evidence sources.
- Ability to develop and communicate clear rationales for feasibility assumptions and recommendations.
- Ability to manage concurrent deliverables, stakeholders, priorities, and deadlines.
- Advanced proficiency in Microsoft Excel, PowerPoint, and Word.
- Confidence working with web-based data, intelligence, and analytics platforms.
- Working knowledge of ICH-GCP principles.
- Postgraduate degree in life sciences, public health, epidemiology, data science, or a related discipline is preferred.
- Global clinical-trial experience, experience in oncology or rare disease, and familiarity with clinical-trial intelligence, epidemiology, site-performance, or claims and real-world-data platforms are preferred.
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.
- Analyze competitive landscapes, historical recruitment, standard of care, treatment landscapes, epidemiology, countries, sites, and patient pools.
- Translate evidence into country, site, enrollment, and operational recommendations.
- Develop rationales for assumptions and identify data limitations and feasibility risks.
- Present feasibility methods, findings, recommendations, and supporting rationale to colleagues, proposal teams, and clients.
- Collaborate with internal colleagues, external consultants, data partners, investigators, and sites to gather and interpret information.
- Plan, coordinate, and analyze targeted site and investigator outreach as appropriate.
- Participate in bid-defense meetings and client discussions.
- Contribute to feasibility methods, data sources, tools, templates, and best practices, and support colleague development.
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