Feasibility Manager

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

📋 Description

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

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

• Conduct and synthesize analyses of competitive landscapes, historical recruitment, standard-of-care, treatment landscapes, epidemiology, country specifics, site details, and patient pools.

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

• Develop logical and transparent rationales for assumptions while identifying significant data limitations and feasibility risks.

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

• Collaborate with internal colleagues, 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.

• 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 development of colleagues within the Feasibility team.

• Operate effectively across various functions, therapeutic areas, and geographical regions.

• Contribute to initiatives that enhance 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 discipline.

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

• 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 accepted.

• 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 capabilities, with the ability to synthesize multiple sources of evidence.

• Ability to create and communicate clear rationales for feasibility assumptions and recommendations.

• Strong attention to detail while remaining mindful of the overall study strategy.

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

• Excellent 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 ownership of the quality, accuracy, and timeliness of deliverables.

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

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

• Working knowledge of ICH-GCP principles.

🏝️ Benefits

• Comprehensive health benefits package.

• Opportunities for professional development and career advancement.

• Flexible working arrangements to promote work-life balance.

• Engaging work environment with a focus on collaboration and innovation.