Feasibility Manager

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

📋 Description

• Lead or participate in feasibility evaluations for client proposals.

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

• Execute and summarize analyses on competitive landscapes, historical recruitment data, standard-of-care practices, treatment environments, epidemiology, country specifics, site details, and patient pools.

• Convert evidence into concise 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 teams, proposal teams, and clients.

• Collaborate with internal team members, external consultants, data partners, investigators, and sites to collect and analyze feasibility information.

• Plan, organize, and evaluate targeted outreach to sites and investigators as necessary.

• Engage in bid-defense meetings and client discussions.

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

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

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

• Contribute to projects that enhance 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 assessments and identifying sites or countries.

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

• Professional fluency in both written and spoken English.

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

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

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

• Familiarity with ICH-GCP principles.

• Ability to synthesize information from multiple evidence sources.

• Capacity to manage several concurrent deliverables, stakeholders, priorities, and deadlines.

🏝️ Benefits

• Fully remote work arrangement.

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

• Equal opportunity employment.

• Reasonable accommodations available during the application process.