Clinical Research Coordinator – Chicago, IL Growing Clinical Research Site Network

Green Life Science; Chicago (IL); On-site; USD 60,000 - 80,000; Full time

Job summary

Green Life Science is seeking a Clinical Research Coordinator in Chicago, IL. The role focuses on coordinating day-to-day clinical trial activities, supporting screening and patient visits, and maintaining meticulous study documentation.

You will collaborate with investigators, sponsors, and CROs to ensure compliance with ICH-GCP and FDA protocols. The position requires CRC or clinical research experience across Phase I–IV studies, with flexibility for contract or interim work.

Qualifications

• CRC/clinical research experience required.
• Experience across Phase I–IV studies.
• Strong knowledge of GCP and FDA regulations.
• Experience across any therapy area is acceptable.
• Contract/interim work available for candidates.

Responsibilities

• Coordinate day-to-day clinical trial activities.
• Support screening, recruitment and patient visits.
• Maintain accurate study documentation and data.
• Work closely with PIs, Sub-Is, sponsors and CROs.
• Support monitoring visits, audits and study close-out.
• Ensure compliance with ICH-GCP, FDA regulations and protocols.

Skills

CRC experience

Clinical research

GCP knowledge

Regulatory knowledge

Project coordination

Job description

Clinical Research Coordinator – Chicago, IL

Location: Chicago, Illinois

About The Role

We’re working with a growing clinical research site network looking for experienced Clinical Research Coordinators (CRCs) to support ongoing and upcoming clinical trials.

What you’ll be doing

• Coordinate day-to-day clinical trial activities
• Support screening, recruitment and patient/subject visits
• Maintain accurate study documentation and data
• Work closely with PIs, Sub-Is, sponsors and CROs
• Support monitoring visits, audits and study close-out
• Ensure compliance with ICH-GCP, FDA regulations and protocols

We’re looking for

• Previous CRC / clinical research experience
• Experience across Phase I–IV studies
• Strong knowledge of GCP and clinical trial processes
• Experience across any therapeutic area
• Candidates available for contract / interim work