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ICON plc

Clinical Trial Liaison

ICON plc

Clinical Trial Liaison advancing patient recruitment and enrollment strategies for ICON, a global clinical research organization. Analyzing trial data and supporting sponsors, investigators, and study participants.

Posted 8/20/2026full-timeRemote • Pennsylvania • 🇺🇸 United StatesMid-LevelSeniorWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in clinical trial enrollment strategies, data analysis, and compliance with regulatory standards. Strong ability to foster relationships with stakeholders and optimize trial outcomes through effective communication and problem-solving.

Highest-signal resume keywords
Clinical Trial EnrollmentData AnalysisRegulatory ComplianceInterpersonal SkillsProblem-Solving

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Data InterpretationClinical Trial Data AnalysisEnrollment Strategy DevelopmentAccuracy Assurance
Soft Skills
Communication SkillsRelationship BuildingDetail-Oriented
Industry Keywords
Life SciencesHealthcarePatient RecruitmentStudy SitesInvestigators

About the role

Key responsibilities & impact
  • Collaborate with cross-functional teams to design and implement effective clinical trial enrollment strategies
  • Analyze and interpret clinical trial data, ensuring accuracy and compliance with regulatory standards
  • Foster strong relationships with study sites and investigators to enhance patient recruitment and retention
  • Act as a liaison between sponsors, investigators, and study participants, providing support and guidance throughout the enrollment process
  • Contribute to the continuous improvement of enrollment processes and strategies to optimize trial outcomes

Requirements

What you’ll need
  • Bachelor's degree in a relevant field, such as life sciences or healthcare
  • Proven experience in clinical trial enrollment or related roles
  • Strong analytical and problem-solving skills with the ability to interpret complex medical data
  • Excellent communication and interpersonal skills to build and maintain effective relationships with stakeholders
  • Detail-oriented with a commitment to ensuring accuracy and compliance in all aspects of clinical trial enrollment
  • 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