Clinical Trial Liaison

🕒 August 26

🌲 North Carolina, Ohio, +2 more states – Remote

🌲 North Carolina – Remote 🏈 Ohio – Remote 🌴 South Carolina – Remote 🎸 Tennessee – Remote

💵 $110.5k - $138.2k / year

⏰ Full Time

🟡 Mid-level

🟠 Senior

👻 Ghost score 14%

What it means: how likely this posting is sitting open without active hiring.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

• Manage the full spectrum of investigator engagement from identification and qualification through enrollment, database lock, and study closeout • Ensure investigators understand protocol intent, scientific rationale, and patient eligibility requirements • Develop strategic relationships with investigators across trials and therapeutic areas • Create tailored recruitment strategies and identify opportunities to reach new patients and accelerate enrollment • Capture site insights to optimize feasibility, protocol design, and study conduct • Lead site-level strategy and risk planning for enrollment and data delivery • Use performance metrics to anticipate issues and maintain clinical milestones • Drive inspection readiness across sites • Collaborate with cross-functional teams and vendors to resolve operational barriers • Influence country/site selection and protocol localization through knowledge of local treatment paradigms and standard of care • Provide oversight and quality assurance for vendor monitoring • Lead Post-Marketing Safety Studies where applicable • Cultivate a portfolio of strategically aligned investigators • Conduct data-informed site prospecting and prioritization • Act as liaison between field teams, vendors, and investigators • Partner with field team colleagues to improve investigator relationships and enrollment outcomes

🎯 Requirements

• Bachelor’s degree or equivalent; strong preference for scientific, clinical, or health-related fields • Minimum 5 years of experience in clinical research or pharmaceutical industry • Experience directly interacting with or working with HCPs and clinical sites • Open to up to 60-80% travel during peak times • Oncology experience required • Breast/Gyn experience preferred • Legal right to work in the country where the role is based

🏖️ Benefits

• Competitive base salary and performance related incentives • 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