Feasibility Manager

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

📋 Description

• Lead or assist in conducting feasibility evaluations for client requests for proposals.

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

• Perform and integrate analyses related to competitive landscapes, historical recruitment, standard-of-care, treatment landscapes, epidemiology, countries, sites, and patient pools.

• Translate evidence into clear recommendations regarding countries, sites, enrollment, and operations.

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

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

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

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

• Take part 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 team members within the Feasibility team.

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

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

⛳️ 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 assisting with clinical trial feasibility analyses and site or country identification.

• 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 considered.

• Experience supporting global clinical trials is preferred.

• Background 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 claims and real-world data platforms is preferred.

• Strong analytical and critical thinking abilities, with a talent for synthesizing multiple sources of evidence.

• Ability to develop and communicate 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 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 escalation when necessary.

• Working knowledge of ICH-GCP principles.

🏝️ Benefits

• Comprehensive health and wellness benefits.

• Opportunities for professional growth and advancement.

• Collaborative and dynamic work environment.

• Access to cutting-edge tools and technologies.

• Flexible work arrangements.