Senior Clinical Research Coordinator — On-Site Trials

Revival Research Institute, LLC; Cary (NC); On-site; USD 65,000 - 90,000; Full time

Job summary

Revival Research Institute, LLC is seeking an experienced site-based clinical research coordinator to independently manage industry-sponsored interventional trials from initiation to close-out. The role requires coordinating study tasks, ensuring regulatory compliance, and supporting investigators and staff on a multi-study load.

Responsibilities include screening and enrollment, data management in EDC, regulatory documentation, sponsor/IRB communications, and participant confidentiality in line

Qualifications

• Requires 2+ years as a Clinical Research Coordinator on industry-sponsored interventional trials.
• Experience obtaining informed consent on interventional protocols.
• Hands-on experience with EDC platforms and data management.
• Knowledge of ICH-GCP, FDA regulations and HIPAA.
• On-site Cary, NC work eligibility.

Responsibilities

• Screen, recruit, and enroll participants per protocol.
• Manage data entry into EDC and resolve queries.
• Maintain trial regulatory binders and quality systems.
• Coordinate sponsor/IRB communications and regulatory submissions.
• Oversee product accountability and study supplies.
• Uphold participant confidentiality and HIPAA standards.

Skills

Clinical Research Coordination

Informed Consent

EDC Data Entry

Monitoring Visits

Regulatory Knowledge

Documentation

On-site Cary work

Education

Master's degree in health field

Tools

EDC platforms

MS Office

Job description

Revival Research Institute, LLC is seeking an experienced site-based clinical research coordinator to independently manage industry-sponsored interventional trials from initiation to close-out. The role requires coordinating study tasks, ensuring regulatory compliance, and supporting investigators and staff on a multi-study load.

Responsibilities include screening and enrollment, data management in EDC, regulatory documentation, sponsor/IRB communications, and participant confidentiality in line