About this opportunity
ICON lists this Clinical Trial Liaison opportunity in clifton, Texas. Review the employer’s description below for duties, qualifications and application requirements.
Job description
ICON seeks a Clinical Trial Liaison to manage investigator relationships and oversee site-level strategy for clinical trials in the Mid-Atlantic and Southeast regions. The role combines clinical investigator management, trial operations, and cross-functional collaboration to optimize enrollment and data delivery.
Responsibilities
Manage investigator identification, qualification, enrollment, and study closeout across trials
Develop and maintain strategic relationships with clinical investigators spanning multiple therapeutic areas
Co-create targeted recruitment strategies to optimize patient enrollment at priority sites
Lead site-level strategy and risk planning to ensure consistent enrollment and data quality
Serve as liaison between field teams, vendors, and investigators to align priorities and resolve operational barriers
Requirements
Bachelor's degree 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
Oncology expertise required; breast/gynecology experience preferred
Willingness to travel 60-80% during peak periods
Legal authorization to work in the United States
Compensation:
$110,520-$138,150 base
#J-18808-Ljbffr
Worksite address
clifton, TX, 76634, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.