Clinical Research Associate

About the role

ICON is a leading healthcare intelligence and clinical research organization. We foster an inclusive environment and welcome applications from individuals who share our commitment to innovation and excellence.

Responsibilities

• Serve as the primary point of contact between investigational sites and the sponsor
• Conduct all types of site visits, including selection, initiation, routine monitoring, and close-out
• Ensure site compliance with ICH-GCP, SOPs, and regulations
• Maintain up-to-date documentation in CTMS and eTMF systems
• Support and track site staff training and maintain compliance records
• Monitor patient safety, ensuring timely and accurate AE/SAE/PQC reporting
• Support subject recruitment and retention efforts at the site level
• Oversee drug accountability and ensure proper storage, return, or destruction
• Resolve data queries and drive timely, high-quality data entry
• Document site progress and escalate risks or issues to the clinical team
• Avoidance of travel for on-site monitoring visits

Requirements

• Graduate with a Bachelor’s degree in Life Sciences or equivalent, or a qualified RNE
• Eligible to work in United States without visa sponsorship
• At least 2+ years of on-site monitoring experience in the pharmaceutical or CRO industry
• Experience monitoring early development Phase I/II clinical studies, across multiple therapeutic areas
• Proficient in ICH-GCP, local regulatory requirements, and clinical systems like CTMS and eTMF
• A clear communicator, problem-solver, and collaborative team player
• Willing and able to travel up to 60% for on-site monitoring visits across the West region; preference given to candidates residing in West region near major HUB airports to support efficient regional travel

Qualifications

Not specified

Skills

Not specified

Benefits

Visit our careers site to read more about the benefits ICON offers.

Pay

$91,336.00-$114,170.00

Schedule

Not specified