Nephrology Clinical Research Coordinator I

Henry Ford Health; Detroit (MI); On-site; USD 45,000 - 65,000; Full time

Job summary

Henry Ford Health in Detroit, MI is seeking a detail-oriented Research Study Coordinator I to support nephrology clinical trials. You will coordinate recruitment, consent, visits, and data collection while ensuring regulatory compliance and patient care.

You will maintain study documentation, work with EHRs and trial management systems, and collaborate with investigators and staff to meet study timelines and quality standards.

Qualifications

• Minimum 1–2 years of experience in clinical research coordination or related healthcare research environment.
• Strong knowledge of clinical research operations, study protocols, and regulatory compliance standards (GCP, IRB).
• Proficiency with EHR systems and clinical trial management software.

Responsibilities

• Coordinate day-to-day operations of nephrology studies including recruitment, screening, enrollment and follow-up.
• Prepare and maintain study documentation, CRFs and regulatory files per GCP and IRB requirements.
• Collect, organize and verify study data ensuring data integrity and accuracy.

Skills

Clinical research coordination

Regulatory compliance (GCP, IRB)

EHR systems proficiency

Study protocol knowledge

Data accuracy and integrity

Organizational & time management

Effective communication

Independence and teamwork

HIPAA compliance

Nephrology knowledge

Job description

Henry Ford Health in Detroit, MI is seeking a detail-oriented Research Study Coordinator I to support nephrology clinical trials. You will coordinate recruitment, consent, visits, and data collection while ensuring regulatory compliance and patient care.

You will maintain study documentation, work with EHRs and trial management systems, and collaborate with investigators and staff to meet study timelines and quality standards.