Senior Clinical Research Program Coordinator

UCLA Health and David Geffen School of Medicine; Charleston (SC); On-site; USD 52,000 - 88,000; Full time

Job summary

Medical University of South Carolina in Charleston, SC, is seeking a Research Program Coordinator II–Journeyman to lead and oversee multiple complex clinical studies. You will work with investigators, study staff, and sponsors to ensure regulatory compliance and study integrity from inception to close.

The role includes trial coordination, data management, patient interactions, enrollment, and reporting to IRB and sponsors.

Qualifications

• A bachelor's degree and three years of relevant program experience.

Responsibilities

• Review research protocols and prepare budgets for IRB/FDA submission; ensure compliance.
• Coordinate data management; ensure timely data entry and monthly PI status reports.
• Liaise with patients, PI, nurses, and sponsors; manage enrollment and scheduling.
• Monitor regulatory documents; report adverse events and protocol deviations to appropriate agencies.
• Support grant writing and dissemination; develop conference materials.
• Assist with study startup, sub-site coordination, and multicenter enrollment.

Job description

Medical University of South Carolina in Charleston, SC, is seeking a Research Program Coordinator II–Journeyman to lead and oversee multiple complex clinical studies. You will work with investigators, study staff, and sponsors to ensure regulatory compliance and study integrity from inception to close.

The role includes trial coordination, data management, patient interactions, enrollment, and reporting to IRB and sponsors.