At ICON, we understand the mounting pressures facing investigative sites. With rising patient burden, increasing protocol complexity, and persistent recruitment challenges, sites are stretched thin—often lacking the bandwidth to run trials effectively. Our Site Engagement solution is designed to address these realities head-on, transforming site relationships into strategic assets that accelerate study delivery and elevate trial outcomes.
The challenge: a strained ecosystem
Clinical research is facing unprecedented strain:
-
53%
of sites report they no longer have capacity to run trials -
70%
cite increased study execution burden -
45%
of study delays stem from recruitment difficulties -
47%
of sites under-enrol or fail to enrol patients
The ICON solution: Site engagement
-
50%
faster to first patient randomised -
50%
increase in patients screened per site per month -
80%
of currently active studies are meeting or exceeding enrolment -
72%
reduction in screen failure rates
We deliver:
- Increased site activation and engagement
- On-site and remote support tailored to site needs
- Strategic insights to drive decision-making
- Quality site selection and relationship management
- Customised recruitment strategies and patient pathway mapping
Expertise that moves the needle
Site Engagement Liaisons (SELs)
Remote site support and solutions to drive patient recruitment
- Support site-specific recruitment funnel
- Drive site understanding and utilisation of resources
- Connect sites to local patient advocacy, community & disease focused funnels
Clinical Trial Liaisons (CTLs)
Doctoral-level professionals who provide global scientific support through trusted peer-to-peer relationships with investigative teams
- On-site investigator engagement
- Intra-institutional & multi-disciplinary expertise
- Differentiate mechanism of action (MOA) & trial impact from competitors
- Field insights to drive efficiency and decision making
Partner with us
Partner with ICON Site Engagement to optimise your site strategy and accelerate your study timelines.
In this section
- Asset Development Consulting
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Blended Solutions
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Cardiac Safety Solutions
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Clinical & Scientific Operations
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Accelerated study start-up
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Biostatistics and Programming
- Clinical Operations
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Data Monitoring Committee Services
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Clinical Supplies Management
- COVID-19
- Clinical data science
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Endpoint Adjudication Services
- Global Logistics
- Interactive Response Technology
- Investigator Payments
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Medical Affairs
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Medical Call Centre Services
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Medical Writing & Publishing
- Pharmacovigilance
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Project and Program Management
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Accelerated study start-up
- Commercial Positioning
- Decentralised Clinical Trials
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Early Clinical
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Accelerated Pharmaceutical Solutions
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Bioanalytical Laboratories
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Biometrics
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Clinical Pharmacology
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Clinical Research Facilities
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Early Phase Oncology
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Ethnic Bridging Studies
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Medical Affairs
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Early Phase Patient Studies
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Early Phase Obesity Trials
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Quality and Compliance
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TQT studies
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Quantitative Pharmacology and Pharmacometrics
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Volunteer Recruitment
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Accelerated Pharmaceutical Solutions
- Language Services
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Laboratories
- Bioanalytical Laboratories
- Central Laboratories
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Specialty Laboratories
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Laboratory Facilities
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Biomarker testing portfolio
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Biospecimen Services
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Biotech Laboratory Solutions
- Medical Imaging
- Outcome Measures
- Real World Intelligence
- Regulatory Affairs
- Symphony Health data
- Site & Patient Solutions
- Strategic Solutions
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Technologies