Feasibility Manager

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

📋 Description

• Lead or participate in conducting feasibility assessments for client requests for proposals.

• Review clinical protocols, study assumptions, client information, and operational plans for both United States and global clinical trials.

• Conduct and synthesize analyses on competitive landscape, historical recruitment, standard-of-care, treatment landscape, epidemiology, country, site, and patient pool.

• Convert evidence into clear recommendations regarding country, site, enrolment, and operational strategies.

• Formulate logical and transparent rationales for assumptions, while identifying critical data limitations and feasibility risks.

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

• Collaborate with internal teams, external consultants, data partners, investigators, and sites to gather and analyze feasibility data.

• Plan, coordinate, and analyze targeted outreach to sites and investigators as necessary.

• Participate in bid-defence meetings and discussions with clients.

• Contribute to the ongoing development of feasibility methods, data sources, tools, templates, and best practices.

• Share expertise and support the professional growth of colleagues within the Feasibility team.

• Work effectively across various functions, therapeutic areas, and geographic regions.

• Contribute to initiatives that enhance Precision for Medicine’s scientifically driven approach and client offerings.

⛳️ Requirements

• Bachelor’s degree in life sciences or a related field.

• A minimum of two years of relevant experience in clinical trial feasibility, clinical operations, site intelligence, epidemiology, clinical research, or a related area.

• Experience in conducting or contributing to clinical trial feasibility analyses and identifying sites or countries.

• Ability to interpret clinical, scientific, epidemiological, and operational data and formulate clear recommendations.

• Professional proficiency in both written and spoken English.

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

• Experience supporting global clinical trials is preferred.

• Experience 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, with the capacity to synthesize multiple sources of evidence.

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

• Excellent attention to detail while keeping the overall study strategy in mind.

• Capability to manage multiple concurrent deliverables, stakeholders, priorities, and deadlines.

• Exceptional written, verbal, and presentation skills.

• Advanced proficiency 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 working style with the ability to operate effectively in a matrix environment.

• Ability to work independently while appropriately seeking input and escalating issues when necessary.

• Working knowledge of ICH-GCP principles.

🏝️ Benefits

• Comprehensive health insurance plans.

• Generous paid time off and holiday schedule.

• Opportunities for professional development and continuing education.

• Collaborative and inclusive work environment.