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Global drug and device development services

Feasibility Lead

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeRemote

About the Job

Requirements

  • Bachelor’s degree in life sciences, nursing, public health, or a related field.
  • At least 5 years of clinical operations experience in biotech, pharma, or CRO, with extensive experience in country and site feasibility oversight.
  • Demonstrated ownership of country selection and/or site selection recommendations for global studies, with supporting analytical work.
  • Strong quantitative skills, including building enrollment models and country scorecards in Excel and working with trial-landscape and real-world data platforms such as Citeline/Informa, IQVIA, TriNetX, ClinicalTrials.gov, and EU CTIS.
  • Working knowledge of ICH GCP, global regulatory and start-up requirements, and country-level submission and approval timelines.
  • Ability to manage multiple studies and shifting priorities in a fast-moving, lean organization.

Responsibilities

  • Lead country selection strategy and develop data-driven recommendations on country mix, site allocation, and enrollment distribution.
  • Oversee CRO completion of design and execution of feasibility assessments, including protocol-specific feasibility questionnaires, competitive landscape and trial-density analyses, epidemiology and standard-of-care review, and regulatory and start-up timeline mapping by country.
  • Pressure-test enrollment assumptions by triangulating internal performance data, external intelligence sources, and direct site and investigator input.
  • Build and maintain an indication-specific site and investigator landscape across North America, Europe, Asia-Pacific, and Latin America, including academic centers, specialty networks, and high-performing private practices.
  • Lead site identification and qualification, coordinate with CRO partners to run pre-study assessments, and translate findings into transparent, criteria-based selection recommendations.
  • Track and manage site performance history—including enrollment rates, data quality, inspection and audit history, screen-failure patterns, and startup cycle times—and use that history in future selection decisions.
  • Maintain feasibility metrics and enrollment.
  • Present feasibility findings, trade-offs, and recommendations clearly, including where data is limited and which assumptions carry risk.
  • Serve as feasibility point of contact for assigned programs, partnering with study teams from concept through first-patient-in.
  • Manage feasibility and site intelligence vendors and CRO feasibility teams by setting scope, holding quality and timeline standards, and critically reviewing deliverables.
  • Partner with Patient Advocacy and Recruitment on patient-finding, referral pathway, and site-support strategies for indications where the eligible population is scarce or highly competed.

Desired Qualifications

  • Experience in Immunology is highly preferred; dermatology and gastrointestinal experience are nice to have.

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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