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Global drug and device development services

Principal Feasibility Analyst

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeNo salary listed

About the Job

Requirements

  • A bachelor's degree in a scientific or allied health field, or equivalent industry experience, and 7+ years of progressive experience in clinical research, feasibility, clinical operations, or study startup within a sponsor or CRO environment, including at least 5 years of hands-on operational feasibility experience supporting complex studies or programs.
  • Demonstrated experience leading feasibility strategy for complex studies or programs, with a track record of influencing program- or portfolio-level decisions about site selection, enrollment strategy, and study acceleration.
  • Experience working across multiple therapeutic areas or late-phase programs, with increasing strategic accountability.
  • Ability to analyze, synthesize, and interpret complex feasibility, operational, and enrollment data from multiple sources, translating findings into clear conclusions, insights, and actionable recommendations.
  • Advanced proficiency in Excel and other data-driven analysis tools, including experience structuring, analyzing, and presenting data to support feasibility assessments, benchmarking, and enrollment forecasting.
  • Strong verbal and written communication skills, including the ability to clearly present complex, data-driven analyses and recommendations to diverse stakeholder audiences, adapting communication style and level of detail.
  • Demonstrated critical thinking and solution-oriented, creative problem-solving skills.
  • Must have the legal right to work in the country where the role is based.

Responsibilities

  • Lead feasibility strategy and execution at the study level, supporting trial optimization and delivery of key milestones while aligning with broader program objectives and program-level feasibility standards.
  • For assigned programs, take end-to-end feasibility ownership across studies within a disease area while continuing study-level feasibility execution under the strategic oversight of a Director or Associate Director.
  • Synthesize and analyze feasibility, operational, and enrollment data from internal and external sources to understand therapeutic areas, standard of care, disease progression, patient and site profiles, and the competitive landscape.
  • Evaluate the clinical trial landscape and use advanced data mining and analytical approaches, including complex enrollment modeling and forecasting, to develop data-driven enrollment assumptions, risk assessments, and study-level strategic recommendations.
  • Assess changing study inputs, reprioritize work, and adjust feasibility approaches to meet timelines and evolving study needs.
  • Balance multiple studies and last-minute requests while maintaining analytical rigor and clear stakeholder communication.
  • Partner with cross-functional study teams and communicate feasibility insights, assumptions, risks, and recommendations to support study planning, site selection, and enrollment strategy decisions.
  • Deliver data-driven presentations to cross-functional teams and governance forums, clearly articulating feasibility insights, risks, and recommendations, including presenting analyses and responding to senior leadership questions as appropriate.
  • Mentor and guide junior feasibility team members, supporting development of analytical skills, feasibility best practices, and consistency in study-level deliverables.
  • Use operational judgment and clinical trial expertise to identify challenges, anticipate risks, and drive solutions supporting high-quality feasibility execution across assigned studies.
  • Contribute to continuous improvement of feasibility processes, tools, and best practices, sharing study-level insights and lessons learned to inform broader team and program approaches.

About the Company

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Global drug and device development services

This company provides consulting, development, and commercialization support for drugs and medical devices through a global network of offices. Its team across 53 countries offers end-to-end services, from strategy and regulatory work to manufacturing and market access, helping clients shorten development time, lower costs, and raise quality. It differentiates itself with wide geographic reach and a clear focus on reducing time to market and cost while leveraging deep experience across many therapeutic areas. Its goal is to help clients accelerate the development of life-saving products and improve quality of life by delivering reliable information, practical solutions, and solid performance.

Company size
10,001+
Company stage
IPO
Headquarters
Ireland
Founded
1990

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