Feasibility Manager

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

📋 Description

• Lead or assist in assessing feasibility for client proposals.

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

• Perform and integrate analyses of competitive landscapes, historical recruitment, standard-of-care, treatment landscapes, epidemiology, as well as country, site, and patient pool considerations.

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

• Create clear and logical justifications for assumptions while identifying key data limitations and feasibility risks.

• Share findings, methods, recommendations, and supporting rationale with Business Development teams, proposal teams, and clients.

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

• Organize, coordinate, and assess targeted outreach to sites and investigators when needed.

• Engage in bid-defense meetings and client discussions.

• Help enhance the development of feasibility techniques, data sources, tools, templates, and best practices.

• Share insights and assist in the growth of team members within the Feasibility team.

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

• Contribute to initiatives that reinforce Precision for Medicine’s scientifically driven methodology 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 domain.

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

• Capability 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.

• Strong analytical and critical thinking abilities, with the skill to synthesize diverse evidence sources.

• Competence in developing and conveying clear rationales for feasibility assumptions and recommendations.

• Exceptional attention to detail while maintaining an understanding of the overall study strategy.

• Ability to juggle multiple concurrent deliverables, stakeholders, priorities, and deadlines.

• Excellent written, verbal, and presentation capabilities.

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

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

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

• Collaborative work style and the ability to function effectively within a matrix environment.

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

• Familiarity with ICH-GCP principles.

🏝️ Benefits

• Fully remote work setup.

• Opportunity to contribute to intricate clinical programs in oncology and rare diseases.

• Chance to collaborate across functions, therapeutic areas, and geographic regions.

• Opportunities for knowledge sharing and colleague development.