Clinical Trial Liaison

ICON

Austin (TX)

On-site

USD 111,000 - 138,000

Full time

10 days ago

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Job summary

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.

Qualifications

  • 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.

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.

Skills

Clinical research experience
Healthcare provider interaction
Oncology expertise
Travel readiness

Education

Bachelor's degree in scientific/clinical/health field

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

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