Senior Clinical Research Coordinator - Onsite Cary, NC

Revival-Research-Institute,-LL; Cary (NC); On-site; USD 60,000 - 85,000; Full time

Job summary

Revival Research Institute, LLC is seeking an experienced site-based Clinical Research Coordinator to lead assigned protocols from initiation to close-out. You will independently screen, consent, enroll participants and manage data, regulatory binders, and sponsor communications on interventional trials.

The role requires 2+ years of CRC experience, proficiency with EDC, and strong knowledge of ICH-GCP and HIPAA, with a preference for advanced certifications and on-site availability in Cary, NC.

Qualifications

• 2+ years as a Clinical Research Coordinator on industry-sponsored interventional trials.
• Experience obtaining informed consent for interventional protocols.
• Hands-on experience with EDC platforms.
• Monitoring visits experience and resolving monitoring findings.
• Knowledge of ICH-GCP E6(R3), FDA Part 11/50/54/56/312 and HIPAA.
• Phlebotomy competency and IV certification preferred.
• Master's degree or equivalent clinical research site experience.
• Ability to work on-site in Cary, NC.

Responsibilities

• Screening, recruitment, and enrollment of participants.
• Data entry into EDC and monitoring visits.
• Regulatory document organization and quality assurance.
• Sponsor/IRB communication and regulatory reporting.
• Investigational product accountability and storage.
• Maintain ICH-GCP and FDA regulatory knowledge.
• Communicate with participants and protect confidentiality.

Skills

CRC experience

EDC platforms

HIPAA knowledge

ICH-GCP E6(R3)

IV certification preferred

ECG / vitals

MS Office

on-site

Education

Master's degree in health-related field

Tools

EDC platforms

Microsoft Office

Job description

Revival Research Institute, LLC is seeking an experienced site-based Clinical Research Coordinator to lead assigned protocols from initiation to close-out. You will independently screen, consent, enroll participants and manage data, regulatory binders, and sponsor communications on interventional trials.

The role requires 2+ years of CRC experience, proficiency with EDC, and strong knowledge of ICH-GCP and HIPAA, with a preference for advanced certifications and on-site availability in Cary, NC.