Clinical Trial Liaison

About the Role

ICON is seeking a Clinical Trial Liaison to manage the full spectrum of investigator engagement and trial delivery across sites and therapeutic areas. The role combines investigator relationship management, enrollment strategy, site performance oversight, vendor collaboration, and readiness for regulatory inspections, with opportunities to lead end-to-end Post-Marketing Safety studies where applicable.

What You'll Do

• 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, ensuring investigators understand protocol intent, scientific rationale, and patient eligibility.
• Develop and sustain strategic, high-trust relationships with investigators across trials and therapeutic areas; co-create tailored recruitment strategies.
• Proactively identify opportunities to reach new patients and accelerate enrollment at priority sites, including novel site models and community-based initiatives.
• Capture and elevate critical site insights to optimize feasibility, protocol design, and study conduct.
• Lead site-level strategy and risk planning to ensure enrollment and data delivery; leverage performance metrics to anticipate issues and sustain momentum.
• Drive inspection readiness as a continuous discipline across sites; provide oversight for vendor monitoring and escalate risks.
• Collaborate with vendors and cross-functional teams to resolve operational barriers with speed and quality; maintain knowledge of local treatment paradigms to influence country/site selection and protocol localization.
• Lead end-to-end management of Post-Marketing Safety Studies where applicable, in compliance with local regulations.
• Act as a liaison between field teams, vendors, and investigators to ensure alignment and knowledge transfer; support investigator experience and site collaboration.

What We're Looking For

• 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 direct interaction with HCPs and clinical sites.
• Open to up to 60-80% travel during peak times.
• Oncology experience required (lung cancer experience preferred).
• Location: US Southeast.

Compensation & Benefits

• Competitive salary with a diverse culture that rewards high performance and nurtures talent.
• Benefits include various annual leave entitlements, health insurance options, retirement planning offerings, and a Global Employee Assistance Programme.
• Life assurance, flexible country-specific options, childcare vouchers, bike purchase schemes, gym discounts, travel subsidies, and health assessments.
• ICON is committed to inclusion and belonging with equal opportunity for all qualified applicants.