Feasibility Manager

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

📋 Description

• Lead or assist in feasibility evaluations for client proposals.

• Assess clinical protocols, study assumptions, client information, and operational plans for clinical trials in the United States and internationally.

• Conduct and summarize analyses of the competitive landscape, historical recruitment data, standard-of-care practices, treatment environments, epidemiology, country specifics, site characteristics, and patient populations.

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

• Formulate logical and transparent justifications for assumptions while identifying key data limitations and feasibility risks.

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

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

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

• Participate in bid-defense 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 professional development of colleagues within the Feasibility team.

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

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

⛳️ Requirements

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

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

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

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

• Professional proficiency in both written and spoken English.

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

• Strong analytical and critical-thinking capabilities, with the ability to integrate multiple sources of evidence.

• Ability to develop and communicate a coherent rationale for feasibility assumptions and recommendations.

• High attention to detail while remaining cognizant of the overall study strategy.

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

• Excellent written, verbal, and presentation abilities.

• 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 working style with the ability to function effectively in a matrix organization.

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

• 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 complex clinical development programs.

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

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

🏝️ Benefits

• Fully remote work arrangement.

• Opportunity to contribute to complex oncology and rare-disease clinical development programs.

• Equal opportunity employment.

• Reasonable accommodation available during the application process.