ICON

Clinical Trial Liaison

United States · Remote (restrictions not stated) · Full time

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About the role

Description from the employer’s posting. Check the employer’s page for the current version.

EmployerICON
LocationUnited States
Work styleRemote (restrictions not stated)
Employment typeFull time
Employer posted1 Oct 2026

Clinical Trial Liaison - Texas

At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.

As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.

As a Clinical Trial Liaison at ICON, you will design and analyze clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.

What you will do:

Clinical Investigator Management

Accountable for the full spectrum of investigator engagement from identification and qualification through enrollment, and support database lock, and study closeout
Serve as a clinical trial scientific ambassador, ensuring investigators deeply understand protocol intent, scientific rationale, and patient eligibility requirements
Develop and sustain strategic, high-trust relationships with investigators that span trials and therapeutic areas
Influence enrollment by co-creating tailored recruitment strategies aligned with site capabilities, patient population realities, and study objectives
Proactively find opportunities to reach new patients, accelerate enrollment and increase impact at priority sites, including for example, novel site models, community-based research initiatives etc
Capture and elevate critical insights from sites to optimize feasibility, protocol design, and study conduct

Show full description

Clinical Trial Management

Lead site-level strategy and risk planning to ensure strong and predictable enrollment and data delivery
Leverage performance metrics to anticipate issues, intervene decisively, and maintain momentum toward clinical milestones
Drive inspection readiness as a continuous discipline across sites
Collaborate across functions and with vendor partners to resolve operational barriers, ensuring delivery with speed and quality
Maintain advanced understanding of local treatment paradigms and standard of care to influence strategic country/site selection and protocol localization
Provide oversight and 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
Business Management and Engagement
Cultivate a portfolio of strategically aligned, high-impact investigators who consistently prioritize client trials
Enable an exceptional investigator experience by being a responsive, knowledgeable, and valued scientific partner
Collaborate cross-functionally (e.g., Medical, Clinical, Study Delivery) to align on trial and site priorities, troubleshooting challenges with urgency and creativity
Conduct data-informed site prospecting and prioritization, contributing to trial competitiveness and regional strategic execution
Maintain scientific fluency and therapeutic expertise to lead meaningful, solutions-focused discussions with site personnel
Act as a key liaison between field teams, vendors, and investigators, ensuring alignment, shared purpose, and continuous knowledge transfer
Partner closely with field team colleagues to elevate the investigator and site experience, ensuring seamless collaboration and improving enrollment outcomes and Investigator relationships

You are:

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

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits may include:

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

Benefits may vary depending on role and location.

Visit our careers site to read more about the benefits ICON offers.

Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.

If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

Are you a current ICON Employee? Please click here to apply

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