Feasibility Manager

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

📋 Description

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

• Examine 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 practices, treatment environments, epidemiology, country specifics, site information, and patient demographics.

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

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

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

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

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

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

• Aid in the ongoing refinement of feasibility methodologies, data sources, tools, templates, and best practices.

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

• Work efficiently across various functions, therapeutic domains, and geographical regions.

• Contribute to initiatives that enhance 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 similar area.

• Experience in conducting or contributing to clinical trial feasibility assessments and the identification of sites or countries.

• Capacity 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 also be acceptable.

• Strong analytical and critical-thinking abilities, capable of synthesizing multiple sources of evidence.

• Proficiency in developing and articulating clear rationales for feasibility assumptions and recommendations.

• High attention to detail while remaining cognizant of the overall study strategy.

• Ability to manage multiple simultaneous deliverables, stakeholders, priorities, and deadlines.

• Exceptional written, verbal, and presentation abilities.

• Advanced skills 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 working style and effectiveness in a matrix environment.

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

• Familiarity with ICH-GCP principles.

🏝️ Benefits

• Fully remote work arrangement.

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

• Opportunity to collaborate across functions, therapeutic areas, and geographical regions.

• Opportunity to contribute to strategic initiatives and enhance feasibility methodologies, data sources, tools, templates, and best practices.

• Knowledge-sharing and professional development opportunities for colleagues.