Clinical Trial Liaison

Job Summary

IRE is seeking a Clinical Trial Liaison to work remotely for US‑based studies while being based in Houston, Harris County. This role provides scientific and clinical support to investigators, ensuring trial sites run efficiently and meet study goals.

Key Responsibilities

• Serve as the primary site engagement specialist for assigned clinical trials.
• Provide investigators and study staff with scientific expertise, protocol guidance, and regulatory support.
• Facilitate communication between site personnel and ICON’s central teams.
• Monitor site performance, troubleshoot issues, and implement corrective actions.
• Assist with patient recruitment strategies and enrollment tracking.
• Conduct site visits (virtual or on‑site) to ensure compliance with Good Clinical Practice (GCP) and study protocols.
• Prepare and deliver training materials, newsletters, and study updates.
• Collect and relay site feedback to improve study processes.

Qualifications

• Bachelor’s degree in life sciences, nursing, pharmacy, or related field (advanced degree preferred).
• Minimum 3 years of experience in clinical research, site management, or a similar liaison role.
• Strong understanding of clinical trial operations, GCP, and FDA regulations.
• Excellent communication, presentation, and interpersonal skills.
• Ability to work independently and manage multiple sites remotely.
• Proficiency with clinical trial management systems (e.g., CTMS, eTMF).

Compensation

Annual salary: $144,881.40 (fixed).

Location

Remote work for US studies; candidate must reside in Houston, Harris County, TX.

Why Join IRE?

ICON plc is a world‑leading healthcare intelligence and clinical research organization that values inclusivity, innovation, and professional growth. Join a global team shaping the future of clinical development.

Frequently Asked Questions

What does a Clinical Trial Liaison do?

A Clinical Trial Liaison acts as the bridge between study sites and the sponsor, providing scientific guidance, monitoring site performance, and ensuring compliance with protocols and regulations.

Is this position fully remote?

Yes, the role supports US‑based clinical trials remotely, but candidates must be located in Houston, Harris County, Texas.

What qualifications are required?

A bachelor’s degree in a life‑science field, at least three years of clinical research experience, strong knowledge of GCP and FDA regulations, and excellent communication skills.