Feasibility Manager

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

📋 Description

• Lead or assist in feasibility evaluations for client proposal requests.

• Assess clinical protocols, study assumptions, client data, and operational strategies for clinical trials in the United States and globally.

• Perform and synthesize analyses related to competitive landscapes, historical recruitment, standard-of-care practices, treatment environments, epidemiology, country, site, and patient pools.

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

• Create logical and transparent justifications for assumptions while identifying significant data limitations and feasibility risks.

• Communicate feasibility methodologies, results, recommendations, and supporting justifications to Business Development team members, proposal groups, and clients.

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

• Organize, coordinate, and evaluate targeted outreach to sites and investigators as necessary.

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

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

• Share expertise and assist in the development of team members within the Feasibility group.

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

• Support initiatives that enhance Precision for Medicine’s scientifically-based approach and client offerings.

⛳️ Requirements

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

• A minimum of two years of pertinent 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 analysis and identifying suitable sites or countries.

• Proficiency in interpreting clinical, scientific, epidemiological, and operational data and formulating clear recommendations.

• Professional proficiency in both written and spoken English.

• Equivalent combinations of education, qualifications, and relevant experience may be accepted.

• Strong analytical and critical-thinking abilities, with the capacity to integrate various evidence sources.

• Skill in developing and articulating a clear rationale for feasibility assumptions and recommendations.

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

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

• Outstanding written, verbal, and presentation skills.

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

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

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

• Collaborative working style and effectiveness in a matrix environment.

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

• Familiarity with ICH-GCP principles.

• Preferred: postgraduate degree in life sciences, public health, epidemiology, data science, or a related field.

• Preferred: experience in supporting global clinical trials.

• Preferred: experience in oncology, rare diseases, or other intricate clinical development programs.

• Preferred: experience in presenting analyses and recommendations to clients or senior stakeholders.

• Preferred: familiarity with clinical-trial intelligence, epidemiology, site performance, or claims and real-world data platforms.

🏝️ Benefits

• Fully remote work arrangement.

• Opportunity to engage in complex oncology and rare-disease clinical programs.

• Chance to contribute to impactful therapies for patients.

• Equal opportunity employment.

• Reasonable accommodations provided during the application process.