Feasibility Manager

This is a fully remote position, open to applicants in Poland, +6 more countries.

📋 Description

• Provide evidence-based feasibility assessments throughout pre-award, post-award, rescue, and stand-alone projects.

• Create recommendations for countries, sites, patient pools, and recruitment by utilizing clinical, scientific, operational, and data analysis.

• Oversee assigned feasibility deliverables.

• Share analyses and recommendations with internal stakeholders and clients.

• Lead or assist in feasibility assessments for client requests for proposals.

• Evaluate clinical protocols, study assumptions, client details, and operational plans for clinical trials in the United States and globally.

• Perform and summarize analyses of the competitive landscape, historical recruitment data, standard-of-care practices, treatment environments, epidemiology, countries, sites, and patient pools.

• Convert evidence into recommendations regarding countries, sites, enrollment, and operational strategies.

• Formulate rationales for assumptions and identify data limitations and feasibility risks.

• Present methods, findings, recommendations, and supporting justifications to Business Development colleagues, proposal teams, and clients.

• Collaborate with internal team members, external consultants, data partners, investigators, and sites.

• Organize, plan, and analyze targeted outreach to sites and investigators.

• Take part in bid-defense meetings and discussions with clients.

• Contribute to methodologies, data sources, tools, templates, best practices, strategic initiatives, and the development of colleagues in feasibility assessments.

• Collaborate across various functions, therapeutic areas, and geographic regions.

⛳️ Requirements

• A bachelor's degree in life sciences or a related field.

• Minimum of two years of pertinent experience in clinical trial feasibility, clinical operations, site intelligence, epidemiology, clinical research, or a related discipline.

• Experience in conducting or assisting with clinical trial feasibility analysis and identifying sites or countries.

• Capability to interpret clinical, scientific, epidemiological, and operational data and provide clear recommendations.

• Proficient in written and spoken English.

• Equivalent combinations of education, qualifications, and relevant experience may be taken into account.

• Experience supporting global clinical trials is preferred.

• Background in oncology, rare diseases, or other complex clinical development programs is preferred.

• Experience in presenting analyses and recommendations to clients or senior stakeholders is preferred.

• Familiarity with clinical trial intelligence, epidemiology, site performance, or real-world data platforms is preferred.

• Strong analytical and critical thinking abilities.

• Ability to establish and convey a clear rationale for feasibility assumptions and recommendations.

• Excellent attention to detail.

• Capacity to manage multiple simultaneous deliverables, stakeholders, priorities, and deadlines.

• Exceptional written, verbal, and presentation skills.

• Advanced skills in Microsoft Excel, PowerPoint, and Word.

• Confidence in working with web-based data, intelligence, and analytics platforms.

• Strong commitment to the quality, accuracy, and timeliness of deliverables.

• Collaborative approach and ability to function effectively within a matrix environment.

• Ability to work independently while appropriately seeking input and escalation.

• Familiarity with ICH-GCP principles.

🏝️ Benefits

• Competitive salary and performance-based bonuses.

• Comprehensive health and wellness benefits.

• Opportunities for professional development and career advancement.

• Flexible working hours and a supportive work environment.