Senior Clinical Research Coordinator

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

Job summary

ClinLab Solutions Group seeks a Clinical Research Coordinator to lead execution of complex trials in collaboration with Principal Investigators, with independence to manage studies and mentor junior staff.

You will ensure regulatory compliance, protect participant safety, and maintain study documents, while coordinating visits, EDC data entry, and liaison with sponsors.

Qualifications

• 3+ years as CRC at a research site, hospital, or private practice.
• HS Diploma or GED; Bachelor's degree preferred.
• Experience mentoring and training other research staff.
• Experience collecting specimens (blood samples).

Responsibilities

• Oversee other CRCs while managing your own clinical trials from initiation to close-out.
• Independently coordinate high-complexity and/or high-enrollment studies.
• Mentor and train junior CRCs and serve as a resource on assigned projects.
• Recruit, screen, and consent study participants in compliance with protocol.
• Dispense investigational product and monitor adherence to study requirements.
• Collect and process biological specimens; perform vital signs, ECGs, and phlebotomy.
• Schedule and conduct participant visits and assessments per protocol.
• Accurately document and enter data into EDC and resolve queries per FDA guidelines.
• Maintain regulatory binders and ensure preparedness for monitoring visits.
• Track and report adverse events and ensure timely SAE submissions.
• Serve as a liaison with sponsors, monitors, and referring physicians.

Skills

CRC experience

Mentoring

Specimen collection

Data entry (EDC)

Education

HS Diploma

GED

Bachelor's preferred

Tools

EDC systems

Job description

Our client is seeking a Clinical Research Coordinator to lead the execution of complex clinical trials in collaboration with Principal Investigators. This role is ideal for a seasoned coordinator ready to take on independent study management, support high-profile trials, and mentor junior staff. You’ll ensure regulatory compliance, uphold research integrity, and protect participant safety while helping to advance cutting-edge treatments. Candidate will handle some managerial responsibilities.

Responsibilities

• Oversee other CRC's while managing your own clinical trials from initiation to close-out
• Independently coordinate high-complexity and/or high-enrollment studies
• Mentor and train junior CRCs and serve as a resource on assigned projects
• Recruit, screen, and consent study participants in compliance with protocol
• Dispense investigational product and monitor adherence to study requirements
• Collect and process biological specimens; perform vital signs, ECGs, and phlebotomy
• Schedule and conduct participant visits and assessments per protocol
• Accurately document and enter data into EDC and resolve queries per FDA guidelines
• Maintain regulatory binders and ensure preparedness for monitoring visits
• Track and report adverse events and ensure timely SAE submissions
• Serve as a liaison with sponsors, monitors, and referring physicians

Qualifications

• 3+ years as a Clinical Research Coordinator at a research site, hospital, or private practice
• HS Diploma or GED (Bachelors Preferred)
• Experience mentoring and training other research staff
• Experience collecting specimens (blood samples)