Clinical Trial Liaison

ICON plc

. Manage the full spectrum of investigator engagement from identification and qualification through enrollment, database lock support, and study closeout .

Posted 9/23/2026full-timeRemote • Texas • United StatesMid-LevelSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in managing clinical trial processes, including investigator engagement, recruitment strategies, and data delivery. Possesses strong oncology knowledge and the ability to cultivate relationships with healthcare professionals and clinical sites.

Highest-signal resume keywords

Clinical Research ExperienceOncology ExpertiseInvestigator EngagementStrategic Relationship DevelopmentData-Driven Decision Making

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial ManagementProtocol DesignFeasibility AssessmentPerformance Metrics AnalysisRisk PlanningQuality AssurancePost-Marketing Safety StudiesSite ProspectingEnrollment Strategy DevelopmentData Delivery

Soft Skills

CollaborationCommunicationProblem-SolvingLeadershipInterpersonal Skills

Industry Keywords

Healthcare ProfessionalsClinical SitesInvestigator ExperienceTreatment ParadigmsStandard of CareVendor MonitoringCross-Functional TeamsTravel FlexibilityTherapeutic AreasPatient Eligibility

About the role

Key responsibilities & impact

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
Develop strategic relationships with investigators across trials and therapeutic areas
Create tailored recruitment strategies and identify opportunities to reach new patients and 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 progress toward clinical milestones
Drive inspection readiness across sites
Collaborate with cross-functional teams and vendor partners to resolve operational barriers
Maintain understanding of local treatment paradigms and standard of care for country/site selection and protocol localization
Provide oversight and quality assurance for vendor monitoring
Lead Post-Marketing Safety Studies where applicable
Cultivate a portfolio of strategically aligned investigators
Support an exceptional investigator experience as a scientific partner
Conduct data-informed site prospecting and prioritization
Act as a liaison between field teams, vendors, and investigators
Partner with field team colleagues to improve enrollment outcomes and investigator relationships

Requirements

What you’ll need

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)
Oncology experience required (Breast/Gyn experience preferred)
Employment with ICON is contingent upon having the legal right to work in the country where the role is based

Benefits

Comp & perks

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