Feasibility Manager

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

📋 Description

• Provide evidence-based feasibility evaluations across pre-award, post-award, rescue, and standalone projects.

• Integrate clinical and scientific insights with operational intelligence and data analysis.

• Formulate recommendations for country, site, patient pool, and recruitment strategies.

• Collaborate with Business Development, Clinical Operations, Medical teams, and other cross-functional partners.

• Oversee assigned feasibility deliverables.

• Present analyses and recommendations to both internal stakeholders and clients.

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

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

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

• Convert evidence into actionable country, site, enrollment, and operational recommendations.

• Create rationales for assumptions while identifying data limitations and feasibility risks.

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

• Work in collaboration with internal team members, external consultants, data partners, investigators, and clinical sites.

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

• Engage in bid-defense meetings and discussions with clients.

• Contribute to the development of feasibility methodologies, data sources, tools, templates, and best practices.

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

• Function across various functions, therapeutic areas, and geographical regions.

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

⛳️ Requirements

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

• A minimum of two years of pertinent experience in clinical trial feasibility, clinical operations, site intelligence, epidemiology, clinical research, or similar areas.

• Experience in conducting or assisting with clinical trial feasibility analyses and identifying sites or countries.

• Capability 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 a talent for synthesizing diverse evidence sources.

• Ability to articulate a clear rationale for feasibility assumptions and recommendations.

• Keen attention to detail while keeping the overall study strategy in mind.

• Skill in managing multiple concurrent deliverables, stakeholders, priorities, and deadlines.

• Outstanding written, verbal, and presentation skills.

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

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

• Strong commitment to the quality, accuracy, and timeliness of deliverables.

• Collaborative approach with the ability to work effectively in a matrix environment.

• Capacity to work independently while appropriately seeking input and escalating issues as necessary.

• Familiarity with ICH-GCP principles.

• A postgraduate degree in life sciences, public health, epidemiology, data science, or a related field is preferred.

• Experience in supporting global clinical trials is preferred.

• Experience 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.

🏝️ Benefits

• Fully remote work arrangement.

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

• Work alongside clinical trial execution, scientific expertise, laboratory capabilities, and advanced data sciences.

• Equal Opportunity Employer.

• Reasonable accommodations are available during the application process.