Feasibility Manager

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About This Role

Precision Medicine Group is expanding its European team and seeking a Feasibility Manager or Senior Feasibility Associate, with the final job title determined by the chosen candidate's level of experience and responsibility. The position is part of the organization's Feasibility Department, delivering evidence-driven feasibility evaluations across pre-award, post-award, rescue, and stand-alone engagements. The employer combines clinical research execution, laboratory services, advanced data sciences, and scientific expertise to assist life sciences…

Job Description

Responsibilities

• Lead or contribute to feasibility assessments for client requests for proposals
• Review clinical protocols, study assumptions, client materials, and operational plans for global and United States clinical trials
• Examine and synthesize competitive landscapes, historical recruitment rates, standard of care, treatment approaches, epidemiology, countries, sites, and patient pools
• Translate gathered evidence into practical country, site, enrolment, and operational recommendations
• Create logical rationales for assumptions while identifying data limitations and risks
• Present methods, findings, recommendations, and rationales to clients, proposal teams, and business development colleagues
• Partner with internal staff, external consultants, investigators, data partners, and sites to gather and interpret feasibility details
• Coordinate and analyze targeted investigator and site outreach
• Take part in client discussions and bid-defense meetings
• Help develop feasibility data sources, methods, tools, templates, and best practices
• Share knowledge and support the professional growth of colleagues within the feasibility team

Requirements

• Bachelor degree in a life sciences discipline or a related field
• Minimum of two years of relevant professional experience in clinical trial feasibility, site intelligence, clinical operations, epidemiology, or clinical research
• Demonstrated experience in contributing to or conducting clinical trial feasibility analysis and site or country identification
• Capability to interpret clinical, scientific, operational, and epidemiological information to formulate clear recommendations
• Professional proficiency in spoken and written English
• Legal authorization to work in the country of employment without requiring employer sponsorship

Qualifications

• Postgraduate degree in a related discipline such as life sciences, data science, epidemiology, or public health
• Prior experience supporting global clinical trials
• Background working in oncology, rare diseases, or other complex clinical development programs
• Demonstrated experience presenting recommendations and analyses to senior stakeholders or clients
• Familiarity with claims and real-world data platforms, site-performance platforms, epidemiology data, or clinical trial intelligence
• Working knowledge of ICH-GCP principles

Core Skills

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