Feasibility Lead

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🐊 Florida, North Carolina, +1 more states – Remote

🐊 Florida – Remote 🌲 North Carolina – Remote 🔔 Pennsylvania – Remote

⏰ Full Time

🟠 Senior

🧪 Clinical Research

👻 Ghost score 10%

What it means: the chance that no one is really hiring for this job.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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ICON plc

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1990

💼 Consulting

🏥 Healthcare

📦 Logistics

Consulting • Healthcare • Logistics

ICON plc is a global provider of clinical, consulting, and commercial services across various sectors in the healthcare and pharmaceutical industries. They offer a wide range of clinical solutions, including decentralised clinical trials, cardiac safety solutions, early clinical laboratories, and medical imaging. ICON also provides technology solutions that support drug development from early phases to post-marketing. Their therapeutic expertise spans cardiovascular, oncology, internal medicine, and more, with a strong focus on transformative therapies like cell and gene therapies and biosimilars. ICON is recognized as a leading Contract Research Organisation (CRO), regularly providing thought leadership and contributing to industry publications and events. Their services are tailored to optimize clinical trials, offer regulatory intelligence, and deliver real-world evidence through robust data analysis and patient-centric solutions.

📋 Description

• 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 questionnaires, competitive landscape and trial-density analyses, epidemiology and standard-of-care review, and regulatory and start-up timeline mapping • Pressure-test enrollment assumptions using internal performance data, external intelligence, 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 • Lead site identification and qualification with CRO partners and translate findings into criteria-based selection recommendations • Track site performance history, including enrollment rates, data quality, inspection and audit history, screen-failure patterns, and startup cycle times • Maintain feasibility metrics and enrollment data • Present feasibility findings, trade-offs, recommendations, data limitations, and key risks • Serve as feasibility point of contact for assigned programs from concept through first-patient-in • Manage feasibility and site intelligence vendors and CRO feasibility teams, including scope, quality, timelines, and deliverable review • Partner with Patient Advocacy and Recruitment on patient-finding, referral pathway, and site-support strategies

🎯 Requirements

• Bachelor’s degree in life sciences, nursing, public health, or a related field. • 5+ years of clinical operations experience in biotech, pharma, or CRO, with extensive experience in country and site feasibility oversight • Therapeutic experience: Experience in Immunology highly preferred (dermatology, GI - nice to have) • Demonstrated ownership of country selection and/or site selection recommendations for global studies, with the analytical work to support them. • Strong quantitative skills — comfortable building enrollment models and country scorecards in Excel and working with trial-landscape and real-world data platforms (e.g., Citeline/Informa, IQVIA, TriNetX, ClinicalTrials.gov, EU CTIS). • Working knowledge of ICH GCP, global regulatory and start-up requirements, and country-level submission and approval timelines. • Excellent written and verbal communication — able to turn ambiguous data into a clear, defensible recommendation for a senior audience. • Ability to manage multiple studies and shifting priorities in a fast-moving, lean organization • Legal right to work in the country where the role is based

🏖️ Benefits

• Competitive base salary and performance related incentives • Health and wellbeing programmes including medical, dental, and vision coverage where applicable • Retirement and pension plans • Life assurance and disability coverage • Employee assistance programmes and wellbeing resources • Learning and development opportunities through structured training and career pathways

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