Feasibility Manager

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

📋 Description

• Lead or assist in conducting feasibility assessments for client proposal requests.

• Review clinical protocols, study assumptions, client details, and operational plans for both U.S. and global clinical trials.

• Perform and synthesize analyses on competitive landscapes, historical recruitment, standard-of-care practices, treatment landscapes, epidemiology, countries, sites, and patient pools.

• Convert evidence into concise recommendations regarding countries, sites, enrollment, and operations.

• Craft 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 teams, and clients.

• Collaborate with internal staff, 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.

• Engage 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.

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

• 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 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 considered.

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

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

• Strong attention to detail while maintaining a holistic view of the overall study strategy.

• Capability 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 commitment to deliverable quality, accuracy, and timeliness.

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

• Ability to work independently while appropriately seeking input and escalation.

• Working knowledge of ICH-GCP principles.

🏝️ Benefits

• Fully remote work arrangement.

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

• Chance to support meaningful therapies for patients.

• Equal Opportunity Employer.