Feasibility Manager

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

📋 Description

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

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

• Conduct and synthesize analyses on competitive landscape, historical recruitment, standard-of-care, treatment landscape, epidemiology, country, site, and patient-pool.

• Translate evidence into clear recommendations regarding country, site, enrollment, and operations.

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

• Present feasibility methods, findings, recommendations, and supporting rationale to Business Development colleagues, proposal teams, and clients.

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

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

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

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

• Share knowledge and support the growth of colleagues within the Feasibility team.

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

• A minimum of two years of relevant experience in clinical trial feasibility, clinical operations, site intelligence, epidemiology, clinical research, or a related area.

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

• Ability to interpret clinical, scientific, epidemiological, and operational information and formulate clear recommendations.

• Professional proficiency in both written and spoken English.

• Equivalent combinations of education, qualifications, and relevant experience are acceptable.

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

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

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

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

• Excellent written, verbal, and presentation abilities.

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

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

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

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

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

• Working knowledge of ICH-GCP principles.

• Preferred: Postgraduate degree in life sciences, public health, epidemiology, data science, or a related field.

• Preferred: Experience supporting global clinical trials.

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

• Preferred: Experience 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 contribute to complex clinical development programs in oncology and rare diseases.

• Opportunity to collaborate with clinical trial execution, scientific expertise, laboratory capabilities, and advanced data sciences.

• Equal Opportunity Employer.

• Reasonable accommodations available for applicants with disabilities.