Feasibility Manager

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

📋 Description

• Take the lead or assist in feasibility assessments for client proposals.

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

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

• Convert evidence into precise recommendations regarding countries, sites, enrolment, and operational strategies.

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

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

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

• Organize and assess targeted outreach to sites and investigators, as necessary.

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

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

• Share expertise and aid in the growth of colleagues within the Feasibility team.

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

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

⛳️ Requirements

• A 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 similar domain.

• Experience in conducting or assisting with clinical trial feasibility analysis and site or country identification.

• 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 pertinent experience may be taken into account.

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

• Aptitude for developing and communicating clear justifications for feasibility assumptions and recommendations.

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

• Ability to handle multiple concurrent deliverables, stakeholders, priorities, and deadlines.

• Exceptional written, verbal, and presentation skills.

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

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

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

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

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

• Familiarity with ICH-GCP principles.

• Preferred: A postgraduate degree in life sciences, public health, epidemiology, data science, or a related area.

• Preferred: Experience in supporting global clinical trials.

• Preferred: Experience in oncology, rare diseases, or other complex clinical development programs.

• Preferred: Experience in presenting analyses and recommendations to clients or senior stakeholders.

• Preferred: Familiarity with clinical trial intelligence, epidemiology, site performance, or claims and real-world data platforms.

🏝️ Benefits

• Fully remote work arrangement.

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

• Equal opportunity employer.

• Reasonable accommodations available for applicants with disabilities.