Senior On-Site Clinical Research Coordinator

Revival-Research-Institute,-LL; Elgin (IL); On-site; USD 60,000 - 90,000; Full time

Job summary

Revival Research Institute in Illinois seeks an experienced site-based Clinical Research Coordinator to independently manage interventional trials from initiation to close-out. You will oversee screening, scheduling visits, data capture, and regulatory documentation on-site in Elgin.

The role requires 2+ years as a CRC, hands-on EDC use, knowledge of ICH-GCP and 21 CFR parts, and strong communication to sponsors, IRB, and staff. On-site work in Elgin, IL is required.

Qualifications

• Minimum 2+ years as a Clinical Research Coordinator at a research site, serving as primary coordinator on industry-sponsored interventional trials.
• Demonstrated experience independently obtaining informed consent on interventional protocols.
• Hands-on experience with EDC platforms.
• Demonstrated experience hosting monitoring visits and resolving monitoring findings independently.
• Working knowledge of ICH-GCP E6(R3) and 21 CFR Parts 11, 50, 54, 56, and 312, and HIPAA.
• Current phlebotomy competency, as well as IV certification, is preferred.
• Proficiency in conducting physical assessments, including comfort with vital signs and 12-lead ECG acquisition.
• Master's degree in a health-related field, or equivalent clinical research site experience.
• Strong computer proficiency including Microsoft Office (Word, Excel, Outlook); excellent verbal and written communication; ability to work independently, manage competing protocol deadlines, and assume ownership of assigned studies.
• Ability to work on-site in Elgin, Illinois.

Responsibilities

• Screening, recruitment, and enrollment.
• Data and monitoring — enter data in EDC and monitor sponsor timelines.
• Regulatory and quality — maintain trial documents and quality controls.
• Sponsor and IRB communication — prepare regulatory submissions and reports.
• Investigational product accountability — receipt, dispensing, and storage.
• Professional and technical knowledge — stay updated on ICH-GCP and FDA regulations.
• Participant communication and confidentiality — maintain HIPAA-compliant protections.

Skills

Clinical research coordination

Independent work

Regulatory knowledge

Communication

Education

Master's degree in health-related field

Tools

EDC platforms

Microsoft Office

Job description

Revival Research Institute in Illinois seeks an experienced site-based Clinical Research Coordinator to independently manage interventional trials from initiation to close-out. You will oversee screening, scheduling visits, data capture, and regulatory documentation on-site in Elgin.

The role requires 2+ years as a CRC, hands-on EDC use, knowledge of ICH-GCP and 21 CFR parts, and strong communication to sponsors, IRB, and staff. On-site work in Elgin, IL is required.