On-Site Clinical Research Coordinator I | Patient-Centric Trials

Eastern Nephrology Associates (ENA); Wilmington (NC); On-site; USD 32,000 - 36,000; Full time

Job summary

Eastern Nephrology Associates seeks a Clinical Research Coordinator I to support onsite clinical trials in Wilmington, NC. The role focuses on coordinating study activities, ensuring data accuracy, and maintaining regulatory documentation under PI supervision.

The position is patient-facing and requires in-person collaboration with providers and accurate handling of sensitive health information in strict HIPAA compliance. Prior CRP/clinical research experience is preferred.

Qualifications

• 2 to 4 years of healthcare experience or 2 to 4 years as a Clinical Research Assistant, or any combination of the two.
• Certified Medical Assistant required.
• Maintains confidentiality and HIPAA compliance.

Responsibilities

• Coordinate all aspects of clinical research activities for assigned studies at investigative site.
• Ensure data accuracy and timely collection for study timelines and protocol.
• Prepare and submit regulatory documents; perform study-specific procedures per Principal Investigator guidance.
• Maintain essential study documentation and ensure compliance with GCP, ICH, and FDA guidelines.

Skills

Healthcare experience

Certified Medical Assistant

Communication skills

On-call readiness

Tools

Microsoft Office

Job description

Eastern Nephrology Associates seeks a Clinical Research Coordinator I to support onsite clinical trials in Wilmington, NC. The role focuses on coordinating study activities, ensuring data accuracy, and maintaining regulatory documentation under PI supervision.

The position is patient-facing and requires in-person collaboration with providers and accurate handling of sensitive health information in strict HIPAA compliance. Prior CRP/clinical research experience is preferred.