Clinical Trial Liaison

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Logo of ICON plc

ICON plc

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 support, and study closeout • Serve as a clinical trial scientific ambassador, explaining protocol intent, scientific rationale, and patient eligibility requirements to investigators • Develop strategic relationships with investigators across trials and therapeutic areas • Influence enrollment through tailored recruitment strategies aligned with site capabilities, patient populations, and study objectives • Identify opportunities to reach new patients, accelerate enrollment, and increase impact at priority sites • Capture and elevate 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, intervene, and maintain progress toward clinical milestones • Drive continuous inspection readiness across sites • Collaborate with functions and vendor partners to resolve operational barriers • Apply knowledge of local treatment paradigms and standards of care to influence country/site selection and protocol localization • Oversee and provide quality assurance for vendor monitoring, escalating risks proactively • Where applicable, lead end-to-end management of Post-Marketing Safety Studies in compliance with local regulations • Cultivate a portfolio of strategically aligned investigators • Provide a responsive, knowledgeable scientific partnership to investigators • Collaborate with Medical, Clinical, Study Delivery, field teams, vendors, and investigators to align priorities and resolve challenges • Conduct data-informed site prospecting and prioritization • Maintain scientific fluency and therapeutic expertise in discussions with site personnel • Facilitate alignment, shared purpose, and knowledge transfer among field teams, vendors, and investigators • Improve investigator relationships, site experience, 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 the pharmaceutical industry • Experience directly interacting with or working with healthcare professionals and clinical sites • Open to up to 60–80% travel during peak times • Immunology experience required • Must be located in Indiana, Kentucky, North Carolina, Michigan, Ohio, or Illinois • 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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