Clinical Trial Liaison

ICON; Lexington (KY); On-site; USD 90,000 - 130,000; Full time

Job summary

ICON seeks a Clinical Trial Liaison to manage investigator relationships and trial operations for neurology studies in a sponsor-dedicated model. The role involves site engagement, enrollment strategy, and cross-functional collaboration to advance clinical trial execution across multiple states.

Responsibilities include investigator recruitment, enrollment support, tailored recruitment strategies, and guiding site-level strategy to meet milestones while maintaining data delivery and inspection

Qualifications

• Bachelor's degree or equivalent in scientific, clinical, or health-related field.
• Minimum 5 years clinical research or pharmaceutical industry experience.
• Direct experience interacting with healthcare providers and clinical sites.
• Ability to travel 60-80% during peak periods.
• Neurodegenerative disease or Alzheimer's experience preferred.

Responsibilities

• Manage investigator recruitment, qualification, enrollment support, and study closeout activities
• Develop tailored recruitment strategies and foster strategic relationships with clinical sites
• Lead site-level strategy and risk planning to ensure enrollment and data delivery milestones
• Collaborate cross-functionally to resolve operational barriers and maintain trial momentum
• Monitor vendor performance and maintain inspection readiness across sites

Skills

Investigator relationships

Site engagement

Enrollment strategy

Cross-functional collaboration

Vendor management

Education

Bachelor's degree or equivalent in scientific, clinical, or health-related field

Job description

ICON seeks a Clinical Trial Liaison to manage investigator relationships and trial operations for neurology studies in a sponsor-dedicated model. The role involves site engagement, enrollment strategy, and cross-functional collaboration to advance clinical trial execution across multiple states.

Responsibilities

• Manage investigator recruitment, qualification, enrollment support, and study closeout activities
• Develop tailored recruitment strategies and foster strategic relationships with clinical sites
• Lead site-level strategy and risk planning to ensure enrollment and data delivery milestones
• Collaborate cross-functionally to resolve operational barriers and maintain trial momentum
• Monitor vendor performance and maintain inspection readiness across sites

Requirements

• Bachelor's degree or equivalent in scientific, clinical, or health-related field
• Minimum 5 years clinical research or pharmaceutical industry experience
• Direct experience interacting with healthcare providers and clinical sites
• Ability to travel 60-80% during peak periods
• Neurodegenerative disease or Alzheimer's experience preferred