Position Summary:
The Lead Clinical Research Coordinator (Lead CRC) is responsible for managing and coordinating the day-to-day operations of clinical research studies, while also providing site-level leadership, mentorship, and oversight to the coordinator team. Reporting to the Site Manager, the Lead CRC ensures protocol compliance, data integrity, and inspection readiness, and serves as the primary resource and first point of escalation for the coordinator group.
Key Responsibilities:
Recruit, screen, consent, and enroll eligible participants in compliance with study protocols and ethical guidelines.
Leadership Responsibilities:
Serve as the first point of escalation for protocol questions, monitor findings, and routine sponsor and IRB communications, escalating to the Site Manager as needed.
Support the Site Manager with operational coordination, scheduling, and site readiness, and provide coverage in the Site Manager's absence where appropriate.
Qualifications:
Education:
Experience:
Experience with IRB processes, electronic data capture (e.g., REDCap, Medidata), and GCP compliance.
Skills:
Working Conditions:
Physical Requirements:
Ability to stand, walk, sit, use hands, and reach with arms.
Equal Opportunity Employer:
Elite Clinical Network is an equal opportunity employer and does not discriminate on the basis of race, color, religion, gender, gender identity, sexual orientation, national origin, disability, age, or veteran status.
