Clinical Trial Liaison
ICON · Blue Bell +4 more
Clinical OperationsFull-time$111k–$138kCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
This Clinical Trial Liaison role involves managing investigator relationships, developing enrollment strategies, and overseeing site-level trial execution across the Mid-Atlantic region. Responsibilities include protocol implementation, data quality assurance, and cross-functional collaboration to support timely patient recruitment and regulatory compliance in clinical research.
What they're looking for
- 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
What you'll be doing
- 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
Privacy & handoff
This role links to ICON's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.