3 дня назад
Feasibility Manager (Clinical Trials)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Feasibility Manager (Clinical Trials): Developing evidence-based feasibility assessments and country, site, patient-pool, and recruitment recommendations for clinical trials with an accent on clinical interpretation, epidemiology, operational intelligence, and data analysis. Focus on synthesising multiple evidence sources, identifying feasibility risks, presenting recommendations to clients, and coordinating site and investigator outreach.
Location: Fully remote within the UK, Spain, Hungary, Poland, Romania, Serbia, or Slovakia
Company
supports life sciences organizations through clinical-trial execution, scientific expertise, laboratory capabilities, and advanced data sciences.
What you will do
- Lead or contribute to feasibility assessments for client requests for proposals and clinical-trial engagements.
- Review clinical protocols, study assumptions, client information, and operational plans for US and global clinical trials.
- Analyse competitive landscapes, historical recruitment, standards of care, treatment landscapes, epidemiology, countries, sites, and patient pools.
- Translate evidence into clear country, site, enrollment, and operational recommendations while identifying assumptions, data limitations, and feasibility risks.
- Present methods, findings, recommendations, and supporting rationale to internal stakeholders, proposal teams, and clients.
- Coordinate information gathering with consultants, data partners, investigators, and sites, including targeted site and investigator outreach.
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 required.
- Advanced proficiency in Microsoft Excel, PowerPoint, and Word, plus working knowledge of ICH-GCP principles.
Nice to have
- Postgraduate degree in life sciences, public health, epidemiology, data science, or a related discipline.
- Experience supporting global clinical trials or working 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, claims, or real-world-data platforms.
Culture & Benefits
- Fully remote work within the specified European countries.
- Collaboration across functions, therapeutic areas, and geographic regions.
- Opportunities to contribute to feasibility methods, data sources, tools, templates, and best practices.
- Knowledge sharing and professional development within the Feasibility team.
- Work on complex clinical-development programs focused on oncology, rare diseases, and meaningful therapies.
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