CRA II: Cross-Therapy Site Monitoring Pro

ICON Strategic Solutions; Chicago (IL); On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

Annual leave

Health insurance

Retirement planning

Employee assistance program

Life assurance

Childcare vouchers

Job summary

ICON Strategic Solutions in Chicago is seeking a Clinical Research Associate to support site monitoring across multiple therapeutic areas in a sponsor-dedicated model.

You will conduct site visits, ensure ICH-GCP compliance, manage CTMS/eTMF documentation, and collaborate with CTAs, LTMs, CTMs while traveling up to 60–75%.

A life sciences bachelor’s or RN, 2+ years’ on-site monitoring, and strong communication are required; visa sponsorship is not available.

Qualifications

• A life sciences degree or nursing qualification.
• 2+ years of on-site monitoring experience in pharma/CRO.
• Strong communication, problem-solving and teamwork abilities.
• Willingness to travel up to 60–75% for on-site visits.

Responsibilities

• Serve as the primary link between sites and sponsor.
• Perform site visits: selection, initiation, monitoring, close-out.
• Ensure ICH-GCP compliance and regulatory adherence.
• Maintain CTMS/eTMF documentation and logs.
• Monitor safety reporting and data quality; resolve queries.
• Support recruitment and site budget tracking as needed.
• Collaborate with CTAs, LTMs and CTMs across regions.

Education

Bachelor’s degree in Life Sciences or equivalent

Tools

CTMS

eTMF

Job description

ICON Strategic Solutions in Chicago is seeking a Clinical Research Associate to support site monitoring across multiple therapeutic areas in a sponsor-dedicated model.

You will conduct site visits, ensure ICH-GCP compliance, manage CTMS/eTMF documentation, and collaborate with CTAs, LTMs, CTMs while traveling up to 60–75%.

A life sciences bachelor’s or RN, 2+ years’ on-site monitoring, and strong communication are required; visa sponsorship is not available.