ZipRecruiter
Clinical Research Coordinator (Contract-to-Hire)
ZipRecruiter, Chicago, Illinois, United States, 60290
Job Description
About the Role:
We are seeking a Principal 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 serve as a mentor to junior staff. You’ll ensure regulatory compliance, research integrity, and participant safety while helping advance cutting-edge treatments. Candidate will handle some managerial responsibilities.
Pay:
$28 - $36 hourly
Key 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:
Education: Minimum Associate’s Degree (Bachelor’s )
Experience:
4+ years as a Clinical Research Coordinator at a research site, hospital, or private practice
Note: Academic lab-only experience does not qualify
Skills & Competencies:
In-depth knowledge of clinical research regulations and ICH-GCP
Strong leadership, organizational, and critical thinking skills
Proficiency in CTMS and EDC systems
Excellent verbal and written communication
Detail-oriented with a commitment to data accuracy and patient safety
Why Join Us?
We are a mission-driven team committed to excellence, innovation, and community health. As a Principal CRC, you’ll have the opportunity to grow into a leadership role while contributing meaningfully to life-changing research.
Apply now to help shape the future of clinical research.
Eagle Clinical Research is an equal opportunity employer.
About the Role:
We are seeking a Principal 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 serve as a mentor to junior staff. You’ll ensure regulatory compliance, research integrity, and participant safety while helping advance cutting-edge treatments. Candidate will handle some managerial responsibilities.
Pay:
$28 - $36 hourly
Key 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:
Education: Minimum Associate’s Degree (Bachelor’s )
Experience:
4+ years as a Clinical Research Coordinator at a research site, hospital, or private practice
Note: Academic lab-only experience does not qualify
Skills & Competencies:
In-depth knowledge of clinical research regulations and ICH-GCP
Strong leadership, organizational, and critical thinking skills
Proficiency in CTMS and EDC systems
Excellent verbal and written communication
Detail-oriented with a commitment to data accuracy and patient safety
Why Join Us?
We are a mission-driven team committed to excellence, innovation, and community health. As a Principal CRC, you’ll have the opportunity to grow into a leadership role while contributing meaningfully to life-changing research.
Apply now to help shape the future of clinical research.
Eagle Clinical Research is an equal opportunity employer.