Clinical Trial Liaison

🔥 26 minutes ago

🤠 Texas – Remote

🤠 Texas – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

👻 Ghost score 10%

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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 • Serve as a clinical trial scientific ambassador, explaining protocol intent, scientific rationale, and patient eligibility requirements • Develop and sustain strategic relationships with investigators across trials and therapeutic areas • Co-create tailored recruitment strategies and identify opportunities to 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 internal functions and vendor partners to resolve operational barriers • Influence country/site selection and protocol localization through local treatment and standard-of-care expertise • Oversee vendor monitoring and proactively escalate risks • Where applicable, lead end-to-end Post-Marketing Safety Studies in compliance with local regulations • Cultivate a portfolio of high-impact investigators and provide an exceptional investigator experience • Conduct data-informed site prospecting and prioritization • Act as liaison between field teams, vendors, and investigators • Partner with field team colleagues to improve enrollment outcomes and investigator relationships

🎯 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 with experience directly interacting with or working with HCPs and clinical sites • Open to up to 60-80% travel during peak times (travel will vary) • Cardio Metabolic experience required • 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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